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C2981613::disease_excludes_finding
disease_excludes_finding
Which finding is specifically excluded in the diagnosis of disease {subj}?
C2981613
Stage IIIA Digestive System Neuroendocrine Tumor AJCC v7
C0333868
Severe cytologic atypia
Neurofibrillary degeneration (morphologic abnormality)
Trisomy 18 (morphologic abnormality)
Severe cytologic atypia
Squamous metaplasia
2
C5420536::disease_excludes_finding
disease_excludes_finding
Which finding is specifically excluded in the diagnosis of disease {subj}?
C5420536
Advanced Cervical Adenosquamous Carcinoma
C0277565
Local disease
Regional enteritis
Basal pneumonia
Local disease
Nodal block
2
C4725707::disease_excludes_normal_cell_origin
disease_excludes_normal_cell_origin
Which normal cell origin is specifically excluded in the disease {subj}?
C4725707
Extracavitary Primary Effusion Lymphoma
C0032112
Plasma Cells
Phagocytes
Cells.HLA-B27
Plasma Cells
Plasma cells.abnormal marker pattern
2
C0079773::disease_excludes_normal_cell_origin
disease_excludes_normal_cell_origin
Which normal cell origin is specifically excluded in the disease {subj}?
C0079773
Lymphoma, T-Cell, Cutaneous
C0887899
Myeloid Cells
Myeloid precursor cell
Myeloid Cells
Pre-B Lymphocytes
Blood Cells
1
C5855556::disease_excludes_normal_cell_origin
disease_excludes_normal_cell_origin
Which normal cell origin is specifically excluded in the disease {subj}?
C5855556
IgM Monoclonal Gammopathy of Undetermined Significance, Plasma Cell Type
C1516097
B lymphoblast
Monocytoid B-Lymphocyte
CYIG+ lymphocyte
B lymphoblast
Activated B-Lymphocyte
2
C1335388::disease_excludes_normal_tissue_origin
disease_excludes_normal_tissue_origin
Which normal tissue origin is specifically excluded in the disease {subj}?
C1335388
Peripheral Intraneural Angiosarcoma
C0014609
Epithelium
Entire respiratory epithelium
Bile Duct Epithelium
Epidermis
Epithelium
3
C5554988::disease_excludes_normal_tissue_origin
disease_excludes_normal_tissue_origin
Which normal tissue origin is specifically excluded in the disease {subj}?
C5554988
Unresectable Myxofibrosarcoma
C0014609
Epithelium
Epithelium
Epidermis proper
Epidermal Ridge
Transitional epithelium
0
C0206717::disease_excludes_normal_tissue_origin
disease_excludes_normal_tissue_origin
Which normal tissue origin is specifically excluded in the disease {subj}?
C0206717
Olfactory Neuroblastoma
C1708239
Germinal Layer
Structure of germinal epithelium of ovary
Basal Domain of the Epithelium
Peyer Patch Germinal Center
Germinal Layer
3
C4520724::disease_excludes_primary_anatomic_site
disease_excludes_primary_anatomic_site
Which primary anatomic site is specifically excluded in the disease {subj}?
C4520724
Stage III Adult Soft Tissue Sarcoma AJCC v7
C0262950
Skeletal bone
Skeletal muscle structure of head
Skeleton of forearm
Skeletal bone
Bone structure of forearm
2
C1332903::disease_excludes_primary_anatomic_site
disease_excludes_primary_anatomic_site
Which primary anatomic site is specifically excluded in the disease {subj}?
C1332903
Cerebellar Vermis Medulloblastoma
C0037925
Spinal Cord
Spinal cord posterior horn
Spinal nerve root NEC
Spinal Cord
Spinal cord tissue structure
2
C1516417::disease_excludes_primary_anatomic_site
disease_excludes_primary_anatomic_site
Which primary anatomic site is specifically excluded in the disease {subj}?
C1516417
Cervical Large Cell Neuroendocrine Carcinoma
C0460004
Head and neck structure
External nose structure
Chest and abdominal vessels
Upper jaw region
Head and neck structure
3
C5206840::disease_has_abnormal_cell
disease_has_abnormal_cell
Which abnormal cell type is characteristic of the disease {subj}?
C5206840
Unresectable Oropharyngeal Squamous Cell Carcinoma
C1514101
Neoplastic Squamous Cell
Neoplastic Cell
Primitive neuroblastic cell
Lymphosarcoma cell
Neoplastic Squamous Cell
3
C2212014::disease_has_abnormal_cell
disease_has_abnormal_cell
Which abnormal cell type is characteristic of the disease {subj}?
C2212014
Ovarian Mucinous Adenocarcinofibroma
C0334227
Tumor cells, malignant
Entire endometrial glandular cell
Tumor cells, malignant
Vacuolated Malignant Fibroblast
Neoplastic Polygonal Cell
1
C2825773::disease_has_abnormal_cell
disease_has_abnormal_cell
Which abnormal cell type is characteristic of the disease {subj}?
C2825773
Malignant Epithelioid Cell Type Gastrointestinal Stromal Tumor
C1514104
Neoplastic Stromal Cell
Endocrine-Stromal Cell
Primitive neuroblastic cell
Neoplastic Epithelial Polygonal Cell
Neoplastic Stromal Cell
3
C2347926::disease_has_associated_anatomic_site
disease_has_associated_anatomic_site
Which anatomic site is associated with the disease {subj}?
C2347926
Refractory Spinal Cord Neoplasm
C0037925
Spinal Cord
Spinal nerve root S1
Spinal Cord
Spinal cord posterior horn
Cervical Spinal Nerve Root
1
C0033375::disease_has_associated_anatomic_site
disease_has_associated_anatomic_site
Which anatomic site is associated with the disease {subj}?
C0033375
Prolactinoma
C0149543
Base of skull structure
Base of skull structure
Orbital complex of bones - floor
Base of cochlear canal
Base of cochlear duct
0
C1520094::disease_has_associated_anatomic_site
disease_has_associated_anatomic_site
Which anatomic site is associated with the disease {subj}?
C1520094
Vulvar Sebaceous Carcinoma
C1261210
Reproductive system
Reproductive system
Skeletal system
Arterial system
Digestive system subdivision
0
C0279748::disease_has_associated_disease
disease_has_associated_disease
Which other disease is associated with the disease {subj}?
C0279748
Undifferentiated carcinoma of nasopharynx
C0042769
Virus Diseases
B Virus Infection
Flavivirus Infections
Virus Diseases
Coronaviridae Infections
2
C1335509::disease_has_associated_disease
disease_has_associated_disease
Which other disease is associated with the disease {subj}?
C1335509
Prostate Kaposi Sarcoma
C0042769
Virus Diseases
B Virus Infection
Filoviridae Infections
Virus Diseases
Pestivirus Infections
2
C2986686::disease_has_associated_disease
disease_has_associated_disease
Which other disease is associated with the disease {subj}?
C2986686
Ann Arbor Stage IV AIDS-Related Lymphoma
C0009450
Communicable Diseases
Immune System Diseases
Opportunistic Infections
Communicable Diseases
Pneumonia in bacterial diseases classified elsewhere
2
C0302592::disease_has_associated_gene
disease_has_associated_gene
Which gene is associated with the disease {subj}?
C0302592
Cervix carcinoma
C2826017
MIR218-1 wt Allele
MIR218-1 wt Allele
MIR373 wt Allele
MIR191 wt Allele
MIR135B wt Allele
0
C0279628::disease_has_associated_gene
disease_has_associated_gene
Which gene is associated with the disease {subj}?
C0279628
Adenocarcinoma Of Esophagus
C1332804
CTSB gene
LTB gene
CTSB gene
SPIB gene
CTNS gene
1
C0002395::disease_has_associated_gene
disease_has_associated_gene
Which gene is associated with the disease {subj}?
C0002395
Alzheimer's Disease
C1705380
ZFYVE9 wt Allele
WDFY2 wt Allele
SIGLEC9 wt Allele
ARHGEF10 wt Allele
ZFYVE9 wt Allele
3
C5238468::disease_has_finding
disease_has_finding
Which finding is characteristic of the disease {subj}?
C5238468
Locally Advanced Neuroendocrine Neoplasm
C0277565
Local disease
Disseminated scars
Burn shock
Local disease
Bone destruction
2
C4764032::disease_has_finding
disease_has_finding
Which finding is characteristic of the disease {subj}?
C4764032
Recurrent B-Cell Prolymphocytic Leukemia
C0277556
Recurrent disease
Recurrent phimosis
Recurrent disease
Recurrent infections, mild
Relapsing Fever
1
C1335035::disease_has_finding
disease_has_finding
Which finding is characteristic of the disease {subj}?
C1335035
Non-Destructive Post-Transplant Lymphoproliferative Disorder
C0021051
Immunologic Deficiency Syndromes
Immunologic Deficiency Syndromes
Hyper-IgM Immunodeficiency Syndrome, Type 1
Simian Acquired Immunodeficiency Syndrome
Immune System Diseases
0
C0677689::disease_has_molecular_abnormality
disease_has_molecular_abnormality
Which molecular abnormality is characteristic of the disease {subj}?
C0677689
Ann Arbor Stage II Grade 3 Contiguous Follicular Lymphoma
C1516672
Clonal Immunoglobulin Gene Rearrangement
Absence of Biallelic TCRgamma Deletion
Clonal Immunoglobulin Gene Rearrangement
FEV Gene Rearrangement
IGH Gene Rearrangement
1
C5670614::disease_has_molecular_abnormality
disease_has_molecular_abnormality
Which molecular abnormality is characteristic of the disease {subj}?
C5670614
Embryonal Tumor with Multilayered Rosettes, DICER1-Mutated
C4528702
DICER1 Gene Mutation
Deleterious DICER1 Gene Mutation
DICER1 Gene Mutation
DOT1L Gene Mutation
DIS3 Gene Mutation
1
C0281700::disease_has_molecular_abnormality
disease_has_molecular_abnormality
Which molecular abnormality is characteristic of the disease {subj}?
C0281700
Stage I Childhood Burkitt Lymphoma
C1516673
Clonal Immunoglobulin Heavy Chain Gene Rearrangement
Absence of Biallelic TCRgamma Deletion
IGK Gene Rearrangement
T-Cell Receptor Gene Rearrangement
Clonal Immunoglobulin Heavy Chain Gene Rearrangement
3
C5669728::disease_has_normal_cell_origin
disease_has_normal_cell_origin
From which normal cell type does the disease {subj} originate?
C5669728
Extramedullary Disease in Multiple Myeloma Involving the Skin
C1511241
Bone Marrow-Homing Plasma Cell
Bone Marrow-Homing Plasma Cell
Mobilized Peripheral Blood Stem Cell
Neoplastic Medium-Sized Lymphocyte
Neoplastic Small to Medium-Sized B-Lymphocyte Resembling a Centrocyte
0
C4682696::disease_has_normal_cell_origin
disease_has_normal_cell_origin
From which normal cell type does the disease {subj} originate?
C4682696
Stage IIB Penile Cancer AJCC v8
C0014597
Epithelial Cells
Ciliated epithelial cell
Epithelial Cells
Endocrine Cells
Malignant Myoepithelial Cell
1
C5855486::disease_has_normal_cell_origin
disease_has_normal_cell_origin
From which normal cell type does the disease {subj} originate?
C5855486
B Acute Lymphoblastic Leukemia with HLF Rearrangement
C0024264
Lymphocyte
CD105+ lymphocyte
HLE+ lymphocyte
Lymphocyte
B-Lymphocytes, Regulatory
2
C3146256::disease_has_normal_tissue_origin
disease_has_normal_tissue_origin
From which normal tissue does the disease {subj} originate?
C3146256
Stage II Rectal Cancer AJCC v7
C0014609
Epithelium
Oral epithelium tissue specimen
Stratified squamous epithelium
Epidermal basement zone
Epithelium
3
C4727196::disease_has_normal_tissue_origin
disease_has_normal_tissue_origin
From which normal tissue does the disease {subj} originate?
C4727196
Recurrent Gastroesophageal Junction Adenocarcinoma
C0014609
Epithelium
Endothelium
Epidermal Ridge
Epithelium
Ductal Epithelium
2
C1292772::disease_has_normal_tissue_origin
disease_has_normal_tissue_origin
From which normal tissue does the disease {subj} originate?
C1292772
Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative
C0229619
Hemopoietic tissue
All bone marrow of bone organ
Hemopoietic tissue
Entire transplanted bone marrow
Genitourinary lymphoid tissue
1
C4763829::disease_has_primary_anatomic_site
disease_has_primary_anatomic_site
What is the primary anatomic site of the disease {subj}?
C4763829
Metastatic Bladder Plasmacytoid Urothelial Carcinoma
C1508753
Urinary system
Skeletal system.peripheral
Articular system
Urinary system
Entire genitourinary system
2
C1710249::disease_has_primary_anatomic_site
disease_has_primary_anatomic_site
What is the primary anatomic site of the disease {subj}?
C1710249
Superficial Epithelioma with Sebaceous Differentiation
C0036505
Sebaceous Glands
Duct of sebaceous gland
Sebaceous Glands
Sebaceous lobule
Sebaceous gland of areola
1
C3899978::disease_has_primary_anatomic_site
disease_has_primary_anatomic_site
What is the primary anatomic site of the disease {subj}?
C3899978
BCLC Stage C Adult Hepatocellular Carcinoma
C0012240
Gastrointestinal system
Respiratory system subdivision
Upper digestive tract NEC
Gastrointestinal system
Entire digestive system
2
C4553846::disease_is_stage
disease_is_stage
For which disease is {subj} a stage?
C4553846
Stage IV Thyroid Gland Papillary Carcinoma AJCC v8
C4683415
Differentiated Thyroid Gland Carcinoma 55 Years and Older AJCC v8 Stage
Stage I Differentiated Thyroid Gland Carcinoma AJCC v8
Stage IVC Differentiated Thyroid Gland Carcinoma AJCC v7
Stage I Differentiated Thyroid Gland Carcinoma Under 45 Years AJCC v7
Differentiated Thyroid Gland Carcinoma 55 Years and Older AJCC v8 Stage
3
C4683425::disease_is_stage
disease_is_stage
For which disease is {subj} a stage?
C4683425
Stage II Thyroid Gland Papillary Carcinoma Under 55 Years AJCC v8
C4683413
Differentiated Thyroid Gland Carcinoma Under 55 Years AJCC v8 Stage
Stage II Thyroid Gland Follicular Carcinoma Under 55 Years AJCC v8
Stage I Thyroid Gland Papillary Carcinoma Under 55 Years AJCC v8
Stage IVB Differentiated Thyroid Gland Carcinoma AJCC v8
Differentiated Thyroid Gland Carcinoma Under 55 Years AJCC v8 Stage
3
C4553875::disease_is_stage
disease_is_stage
For which disease is {subj} a stage?
C4553875
Stage IVB Differentiated Thyroid Gland Carcinoma AJCC v8
C4683415
Differentiated Thyroid Gland Carcinoma 55 Years and Older AJCC v8 Stage
Stage I Differentiated Thyroid Gland Carcinoma Under 55 Years AJCC v8
Stage II Thyroid Gland Follicular Carcinoma 55 Years and Older AJCC v8
Stage II Thyroid Gland Papillary Carcinoma 55 Years and Older AJCC v8
Differentiated Thyroid Gland Carcinoma 55 Years and Older AJCC v8 Stage
3
C1709312::disease_mapped_to_gene
disease_mapped_to_gene
Which gene is mapped to the disease {subj}?
C1709312
Oncocytic Variant Thyroid Gland Papillary Carcinoma
C1847162
GOLGA5/RET Fusion Gene
HMGA2/LHFP Fusion Gene
HMGA2/CCNB1IP1 Fusion Gene
TFG/NTRK1 Fusion Gene
GOLGA5/RET Fusion Gene
3
C1332471::disease_mapped_to_gene
disease_mapped_to_gene
Which gene is mapped to the disease {subj}?
C1332471
Benign Anal Granular Cell Tumor
C1412687
ATP6AP1 gene
NCKAP1 gene
ATP6AP1 gene
CPA6 gene
CPA1 gene
1
C5854746::disease_mapped_to_gene
disease_mapped_to_gene
Which gene is mapped to the disease {subj}?
C5854746
Childhood Acute Myeloid Leukemia with t(5;11)(q35;p15); NUP98-NSD1
C1847677
NSD1/NUP98 FUSION GENE
HOXD11/NUP98 FUSION GENE
NSD1/NUP98 FUSION GENE
MESDC2/SENP1 FUSION GENE
HOXA9/NUP98 FUSION GENE
1
C1336015::disease_may_have_abnormal_cell
disease_may_have_abnormal_cell
Which abnormal cell type may be found in the disease {subj}?
C1336015
Smoldering Adult T-Cell Leukemia/Lymphoma
C1514093
Neoplastic Small T-Lymphocyte
Neoplastic T-Cell Large Granular Lymphocyte
Neoplastic Small T-Prolymphocyte
Tumor Associated Lymphocyte
Neoplastic Small T-Lymphocyte
3
C5668167::disease_may_have_abnormal_cell
disease_may_have_abnormal_cell
Which abnormal cell type may be found in the disease {subj}?
C5668167
Pericardial Primary Effusion Lymphoma
C1513927
Neoplastic B-Immunoblast
Neoplastic Follicle Center B-Cell
Neoplastic Granulocyte
Neoplastic B-Immunoblast
Neoplastic Myeloid Cell
2
C0855142::disease_may_have_abnormal_cell
disease_may_have_abnormal_cell
Which abnormal cell type may be found in the disease {subj}?
C0855142
Nodal marginal zone B-cell lymphoma stage I
C1514058
Neoplastic Plasma Cell
Neoplastic Glial Cell
Neoplastic Melanocyte
Neoplastic Endocrine Cell
Neoplastic Plasma Cell
3
C0855184::disease_may_have_associated_disease
disease_may_have_associated_disease
Which other disease may be associated with the disease {subj}?
C0855184
Testicular choriocarcinoma stage III
C0010417
Cryptorchidism
Indeterminate sex and pseudohermaphroditism
Cryptorchidism
Opodidymus
Hologastroschisis
1
C5206775::disease_may_have_associated_disease
disease_may_have_associated_disease
Which other disease may be associated with the disease {subj}?
C5206775
Refractory Kidney Medullary Carcinoma
C0037054
Sickle Cell Trait
hemoglobinopathy trait SS
Sickle Cell Trait
Sickle cell arthropathy
Sickle cell beta plus thalassemia
1
C4725616::disease_may_have_associated_disease
disease_may_have_associated_disease
Which other disease may be associated with the disease {subj}?
C4725616
Refractory Ovarian Endometrioid Adenocarcinoma
C0476089
Endometrial Carcinoma
Type II Endometrial Adenocarcinoma
Recurrent Endometrial Undifferentiated Carcinoma
Recurrent Endometrial Endometrioid Adenocarcinoma
Endometrial Carcinoma
3
C1333842::disease_may_have_cytogenetic_abnormality
disease_may_have_cytogenetic_abnormality
Which cytogenetic abnormality may be present in the disease {subj}?
C1333842
Grade 3 Cutaneous Follicular Lymphoma
C1515604
del(6q23)
del(6p21)
del(6q23)
del(8p12p21)
del(11q22.3)
1
C4763841::disease_may_have_cytogenetic_abnormality
disease_may_have_cytogenetic_abnormality
Which cytogenetic abnormality may be present in the disease {subj}?
C4763841
Metastatic Bladder Giant Cell Urothelial Carcinoma
C1517979
Loss of Chromosome 2q
Loss of Chromosome 20
Chromosome 15q, partial deletion
Loss of Chromosome 2q
Chromosome 5q31-33 Deletion
2
C1332997::disease_may_have_cytogenetic_abnormality
disease_may_have_cytogenetic_abnormality
Which cytogenetic abnormality may be present in the disease {subj}?
C1332997
Childhood T Lymphoblastic Leukemia/Lymphoma
C1515789
t(7;9)(q34;q34.3)
t(3;3)(q21.3;q26.2)
t(7;9)(q34;q34.3)
t(13;22)(q22;q13.3)
t(1;19)(q23;p13.3)
1
C1334249::disease_may_have_finding
disease_may_have_finding
Which finding may be present in the disease {subj}?
C1334249
Intraductal Micropapillary Breast Carcinoma
C0520594
Breast Microcalcification
Breast Microcalcification
Cervical Microglandular Hyperplasia
Cortical calcifications
Calcified granuloma
0
C5237826::disease_may_have_finding
disease_may_have_finding
Which finding may be present in the disease {subj}?
C5237826
Advanced Colorectal Adenocarcinoma
C0024050
Lower gastrointestinal hemorrhage
Other neonatal gastrointestinal hemorrhage
Duodenal hemorrhage
Gastrointestinal bleeding neonatal
Lower gastrointestinal hemorrhage
3
C1519915::disease_may_have_finding
disease_may_have_finding
Which finding may be present in the disease {subj}?
C1519915
Vaginal Adenosquamous Carcinoma
C2979982
Vaginal Hemorrhage
Vaginal Hemorrhage
Hemorrhoidal Hemorrhage
Genital hemorrhage
Hemorrhage of tunica vaginalis
0
C1512749::disease_may_have_molecular_abnormality
disease_may_have_molecular_abnormality
Which molecular abnormality may be present in the disease {subj}?
C1512749
Invasive Bladder Urothelial Carcinoma with Trophoblastic Differentiation
C3266989
H-ras gene mutation
KRAS Exon 3 Mutation
Checkpoint kinase 2 gene mutation
NRAS Gene Amplification
H-ras gene mutation
3
C4743673::disease_may_have_molecular_abnormality
disease_may_have_molecular_abnormality
Which molecular abnormality may be present in the disease {subj}?
C4743673
Digestive System Small Cell Neuroendocrine Carcinoma
C1515171
TP53 Gene Inactivation
Deleterious TP53 Gene Mutation
Inactivating RAD51B Gene Mutation
TP53 Gene Inactivation
TGFBR2 Gene Inactivation
2
C1334052::disease_may_have_molecular_abnormality
disease_may_have_molecular_abnormality
Which molecular abnormality may be present in the disease {subj}?
C1334052
Human Papillomavirus-Related Cervical Squamous Cell Carcinoma
C1512127
HER2 gene amplification
HER2 gene amplification
TERT Deficiency
BLyS polymorphism
Hypermelanosis due to hormonal factor
0
C5401025::disposition_of
disposition_of
Which of the following is {subj} a disposition of?
C5401025
Estrogen receptor agonist (disposition)
C0059668
estrone sulfate
estrone sulfate
butacaine sulfate
estradiol valerate compounding powder
nomegestrol and estrogen
0
C5434066::disposition_of
disposition_of
Which of the following is {subj} a disposition of?
C5434066
Alpha-adrenergic and beta-adrenergic agonist (disposition)
C0304430
pseudoephedrine hydrochloride
pseudoephedrine hydrochloride
aminacrine hydrochloride
Methscopolamine nitrate + pseudoephedrine hydrochloride
cinnamedrine hydrochloride
0
C3853002::disposition_of
disposition_of
Which of the following is {subj} a disposition of?
C3853002
Androgen Synthesis Inhibitors
C5686001
Steroidal androgen synthesis inhibitor
testosterone cypionate compounding powder
Calcium antacid compound combinations
Steroidal androgen synthesis inhibitor
Testosterone esters
2
C0185622::do_not_code_with
do_not_code_with
Which of the following should not be coded with {subj}?
C0185622
Open treatment of fracture of orbit, except blowout; with implant
C1609555
Irrigation of implanted venous access device for drug delivery systems
Revision of implantable venous access port
Irrigation of implanted venous access device for drug delivery systems
Implantation of electronic stimulator into urinary bladder
Fluoroscopy guided removal of implantable venous access device
1
C0197419::do_not_code_with
do_not_code_with
Which of the following should not be coded with {subj}?
C0197419
Corneal wedge resection for correction of surgically induced astigmatism
C1609555
Irrigation of implanted venous access device for drug delivery systems
Irrigation of ventricular catheter
Accessing of implantable venous access port
Implantation of spinal drug delivery reservoir
Irrigation of implanted venous access device for drug delivery systems
3
C0812502::do_not_code_with
do_not_code_with
Which of the following should not be coded with {subj}?
C0812502
Laparoscopy, abdomen, peritoneum, and omentum, diagnostic, with or without collection of specimen(s) by brushing or washing (separate procedure)
C1736652
Laparoscopy, surgical, supracervical hysterectomy, for uterus 250 g or less
Total hysterectomy via vaginal approach using intrafascial technique
Laparoscopy, surgical, supracervical hysterectomy, for uterus 250 g or less
laparoscopic vaginal hysterectomy with repair of cystocele and rectocele
laparoscopy with fulguration of gynecologic lesions of uterine surface
1
C0695240::due_to
due_to
Which of the following is {subj} due to?
C0695240
Mechanical complication of gastrostomy
C0017196
Gastrostomy
Gastrostomy
Button gastrostomy feeding
Hepatogastrostomy
Gastroenterostomy
0
C4040068::due_to
due_to
Which of the following is {subj} due to?
C4040068
Hepatic coma due to acute hepatitis C
C0400914
Acute hepatitis C
Hepatitis with hepatic coma
Chronic viral hepatitis D
Acute hepatitis C
Acute hepatopathy
2
C0410706::due_to
due_to
Which of the following is {subj} due to?
C0410706
Osteoporotic kyphosis
C0029456
Osteoporosis
Low turnover osteopathy
Osteopenia or osteoporosis
Osteoporosis
Osteophyte
2
C3887685::enzyme_metabolizes_chemical_or_drug
enzyme_metabolizes_chemical_or_drug
Which chemical or drug is metabolized by the enzyme {subj}?
C3887685
Cytochrome P450 2D6, human
C0282321
propranolol hydrochloride
alprenolol hydrochloride
celiprolol hydrochloride
tulobuterol hydrochloride
propranolol hydrochloride
3
C0535996::enzyme_metabolizes_chemical_or_drug
enzyme_metabolizes_chemical_or_drug
Which chemical or drug is metabolized by the enzyme {subj}?
C0535996
CYP3A5 protein, human
C0006462
buspirone
profenamine
buspirone
Doprin
Buspirone only product
1
C1142644::enzyme_metabolizes_chemical_or_drug
enzyme_metabolizes_chemical_or_drug
Which chemical or drug is metabolized by the enzyme {subj}?
C1142644
cytochrome P450 3A4 protein, human
C0085170
astemizole
astemizole
terizidone
piminodine
tolazamide
0
C1517178::eo_disease_maps_to_human_disease
eo_disease_maps_to_human_disease
Which human disease does the experimental organism disease {subj} map to?
C1517178
Fibroma of the Mouse Skin
C0016045
fibroma
Recurrent fibromatosis
Fascial fibroma
fibroma
fetal myxolipoma
2
C1522089::eo_disease_maps_to_human_disease
eo_disease_maps_to_human_disease
Which human disease does the experimental organism disease {subj} map to?
C1522089
Adenoma of the Mouse Pulmonary System
C0001430
Adenoma
Carcinofibroma
Solid carcinoma
Adenoma
Flat adenoma
2
C1517177::eo_disease_maps_to_human_disease
eo_disease_maps_to_human_disease
Which human disease does the experimental organism disease {subj} map to?
C1517177
Fibroma of the Mouse Intestinal Tract
C0017185
Gastrointestinal Neoplasms
Gastrointestinal Neoplasms
Gastrointestinal Carcinoid Tumor
Jejunal Neoplasms
Gastrointestinal Stromal Tumors
0
C1826983::exhibited_by
exhibited_by
Which of the following exhibits {subj}?
C1826983
5-methyltetrahydrofolate-homocysteine methyltransferase reductase activity
C1453956
MTRR protein, human
MUSK protein, human
LTF protein, human
MTRR protein, human
TPR protein, human
2
C1149833::exhibited_by
exhibited_by
Which of the following exhibits {subj}?
C1149833
feruloyl esterase activity
C0117605
feruloyl esterase
2-ethylmalate synthase
vanillyl-alcohol oxidase
benzoyl-CoA reductase
feruloyl esterase
3
C1151783::exhibited_by
exhibited_by
Which of the following exhibits {subj}?
C1151783
methylenetetrahydrofolate reductase NADPH activity
C0066357
Methylenetetrahydrofolate reductase (NADPH)
Aldose-6-phosphate reductase (NADPH)
CoA-disulfide reductase (NADH)
Methylenetetrahydrofolate reductase (NADPH)
Protein-disulfide reductase (NAD(P)H)
2
C1439099::exhibits
exhibits
Which of the following is exhibited by {subj}?
C1439099
CHST15 protein, human
C1325240
N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase activity
positive regulation of CDP-diacylglycerol-serine O-phosphatidyltransferase activity
formate C-acetyltransferase activity
UDP-glucose:glycoprotein glucosyltransferase activity
N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase activity
3
C1456416::exhibits
exhibits
Which of the following is exhibited by {subj}?
C1456416
MAPK13 protein, human
C1150590
SAP kinase 4 activity
SAP kinase 4 activity
protein kinase A signaling
negative regulation of protein kinase B signaling
protein kinase regulator activity
0
C2001855::exhibits
exhibits
Which of the following is exhibited by {subj}?
C2001855
EPHX1 protein, human
C2247484
cis-stilbene-oxide hydrolase activity
diacetyl reductase ((R)-acetoin forming) activity
cis-stilbene-oxide hydrolase activity
5'-hydroxyaverantin dehydrogenase activity
all-trans-retinyl-ester hydrolase, 11-cis retinol forming activity
1
C0585526::finding_method_of
finding_method_of
Which of the following uses {subj} as a finding method?
C0585526
Exploration of colon
C2182884
descending colon procedure manual abdominal exploration noting liver nodules
Sigmoid colectomy and exteriorisation of bowel NEC
Left hemicolectomy and exteriorisation of bowel NEC
descending colon procedure manual abdominal exploration noting liver nodules
Emergency excision of abnormal appendix NEC
2
C1536105::finding_method_of
finding_method_of
Which of the following uses {subj} as a finding method?
C1536105
Computed Tomography Angiography
C3694981
CT angiography of head: aneurysm in right posterior communicating artery
CT angiography of head: aneurysm in right posterior communicating artery
angiography of cerebral portion of right carotid artery
fluoroscopic angiography of cerebral artery and left internal carotid artery
fluoroscopic angiography of cerebral artery with right carotid artery with IA contrast
0
C0412716::finding_method_of
finding_method_of
Which of the following uses {subj} as a finding method?
C0412716
Magnetic resonance imaging of ankle
C5765162
MRI of tibiocalcaneal ligament
MRI of calcaneus
MRI of acromioclavicular joint
MRI of tibiocalcaneal ligament
MRI of calcaneus, talus, navicular and cuboid bones of foot
2
C0032005::finding_site_of
finding_site_of
Which condition or procedure has {subj} as a finding site?
C0032005
Pituitary Gland
C5568640
Xanthomatous hypophysitis
Pseudomembranous stomatitis
Xanthomatous hypophysitis
Palmoplantar hypohidrosis
Secondary syphilitic osteopathy
1
C0000726::finding_site_of
finding_site_of
Which condition or procedure has {subj} as a finding site?
C0000726
Abdomen
C0206646
Fibromatosis, Abdominal
Fibromatosis, Abdominal
Intra-Abdominal Lymphangioma
Endometrioid adenofibroma, malignant
Cystadenoma, Papillary
0
C0700038::finding_site_of
finding_site_of
Which condition or procedure has {subj} as a finding site?
C0700038
Female Reproductive System
C0346170
Serous cystadenoma of ovary
Schneiderian carcinoma of cervix
Mucinous adenocarcinoma of appendix
Serous cystadenoma of ovary
Papillary serous cystadenoma
2
C1706514::gene_associated_with_disease
gene_associated_with_disease
Which disease is associated with the gene {subj}?
C1706514
GNAI2 wt Allele
C0032000
Pituitary Adenoma
Childhood Parathyroid Gland Adenoma
Pituitary Adenoma
Primary pituitary carcinoma
Pituitary Neoplasms
1
C2825749::gene_associated_with_disease
gene_associated_with_disease
Which disease is associated with the gene {subj}?
C2825749
MIRLET7G wt Allele
C0684249
Carcinoma of lung
Carcinoma of lung
Primary solid carcinoma of lung
Carcinoma of upper gum
Primary carcinoma of penis
0
C1416655::gene_associated_with_disease
gene_associated_with_disease
Which disease is associated with the gene {subj}?
C1416655
KIT gene
C0205851
Germ cell tumor
Extragonadal primary germ cell cancer
Germ cell tumor
Ovarian germ cell polyembryoma
Testicular gonadoblastoma
1
C1336804::gene_encodes_gene_product
gene_encodes_gene_product
Which gene product is encoded by the gene {subj}?
C1336804
Transforming Growth Factor-Beta Family Gene
C0053932
Bone Morphogenetic Proteins
Eosinophil Major Basic Protein
Bone Morphogenetic Proteins
MAGE-A1/MAGE-A3/NY-ESO-1 Peptides Vaccine
Heparan Sulfate Proteoglycans
1
C0017362::gene_encodes_gene_product
gene_encodes_gene_product
Which gene product is encoded by the gene {subj}?
C0017362
Genes, Regulator
C3254737
LRRTM2 protein, human
SEphB4-HSA
BCDX2 Complex
rca protein, plant
LRRTM2 protein, human
3
C1334166::gene_encodes_gene_product
gene_encodes_gene_product
Which gene product is encoded by the gene {subj}?
C1334166
Immunoprotein Gene
C1870106
Immunoglobulin Lambda-Like Polypeptide 1, human
Virus-specific Hyperimmune Globulins
Immune Globulin (Human)
Secretory Immunoglobulin A
Immunoglobulin Lambda-Like Polypeptide 1, human
3
C1709988::gene_in_chromosomal_location
gene_in_chromosomal_location
What is the chromosomal location of the gene {subj}?
C1709988
SMARCD2 wt Allele
C1520781
17q23-q24
14q23-q24.1
3q21-q28
17q23-q24
4q26-q32
2
C3538709::gene_in_chromosomal_location
gene_in_chromosomal_location
What is the chromosomal location of the gene {subj}?
C3538709
DDX3X wt Allele
C1520174
Xp11.3-p11.23
Xp11.3-p11.23
3p24.1-p22
1p36.2-p36.12
17p11.1
0
C1705990::gene_in_chromosomal_location
gene_in_chromosomal_location
What is the chromosomal location of the gene {subj}?
C1705990
LGALS8 wt Allele
C1521015
1q42-q43
13q12-q13
Xq11-q13
1q42-q43
1p32-q12
2
C1708291::gene_involved_in_molecular_abnormality
gene_involved_in_molecular_abnormality
In which molecular abnormality is the gene {subj} involved?
C1708291
CDC73 gene
C1708292
CDC73 Gene Mutation
CDC73 Gene Mutation
PCDH19 gene mutation
JAK Family Gene Mutation
Non-synonymous JAK Family Gene Mutation
0
C1335675::gene_involved_in_molecular_abnormality
gene_involved_in_molecular_abnormality
In which molecular abnormality is the gene {subj} involved?
C1335675
Receptor Tyrosine Kinase Gene
C5447807
ERBB2 NM_004448.3:c.2033G>A
CYP3A4 gene.c.6C>T
Point mutation in exon 21 (L858R)
ERBB2 NM_004448.3:c.2033G>A
NR5A1 gene mutation
2
C0919528::gene_involved_in_molecular_abnormality
gene_involved_in_molecular_abnormality
In which molecular abnormality is the gene {subj} involved?
C0919528
KMT2A gene
C1518132
KMT2A-MLLT1 Fusion Protein Expression
CDX2 Protein Overexpression
KMT2A-MLLT1 Fusion Protein Expression
EGFR gene overexpression
Non-synonymous RAS Family Gene Mutation
1
C1537502::gene_involved_in_pathogenesis_of_disease
gene_involved_in_pathogenesis_of_disease
In the pathogenesis of which disease is the gene {subj} involved?
C1537502
KRAS gene
C1335167
mucinous adenocarcinoma of ovary
mucinous adenocarcinoma of oral cavity
mucinous adenocarcinoma of ovary
mucinous adenocarcinoma of anal canal
mucinous adenocarcinoma of breast
1
C0079419::gene_involved_in_pathogenesis_of_disease
gene_involved_in_pathogenesis_of_disease
In the pathogenesis of which disease is the gene {subj} involved?
C0079419
TP53 gene
C1332166
Adenocarcinoma of the gastroesophageal junction
Primary carcinoma of lower third of esophagus
Adenocarcinoma of the gastroesophageal junction
Adenocarcinoma of duodenum
Basal cell carcinoma of esophagus
1