Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0041315
Disease: Tuberculosis, Laryngeal
Tuberculosis, Laryngeal
1 0 1 0.11 0 0
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia
1 0 1 0.11 0 0
CUI: C0231246
Disease: Failure to gain weight
Failure to gain weight
1 0 1 0.11 0 0
CUI: C0238293
Disease: Osteomyelosclerosis
Osteomyelosclerosis
1 0 1 0.11 0 0
CUI: C0276658
Disease: Infection by Aspergillus flavus
Infection by Aspergillus flavus
1 0 1 0.11 0 0
CUI: C0349398
Disease: Paranoid delusion
Paranoid delusion
1 0 1 0.11 0 0
CUI: C0432240
Disease: Stuve-Wiedemann dysplasia
Stuve-Wiedemann dysplasia
1 0 1 0.11 0 0
CUI: C0456877
Disease: High grade T-cell lymphoma
High grade T-cell lymphoma
1 0 1 0.11 0 0
CUI: C0457928
Disease: Bent bone dysplasia group
Bent bone dysplasia group
1 0 1 0.11 0 0
CUI: C0853398
Disease: Endocarditis enterococcal
Endocarditis enterococcal
1 0 1 0.11 0 0
CUI: C1096446
Disease: Slight temperature
Slight temperature
1 0 1 0.11 0 0
Refractory Mature T-Cell and NK-Cell Non-Hodgkin Lymphoma
1 0 1 0.11 0 0
CUI: C1832146
Disease: Metaphyseal rarefaction
Metaphyseal rarefaction
1 0 1 0.11 0 0
CUI: C1857139
Disease: Abnormal metaphyseal trabeculation
Abnormal metaphyseal trabeculation
1 0 1 0.11 0 0
Macular hypopigmented whorls, streaks, and patches
1 0 1 0.11 0 0
LEUKEMIA, PHILADELPHIA CHROMOSOME-POSITIVE, RESISTANT TO IMATINIB
1 0 1 0.11 0 0
CUI: C4023165
Disease: Abnormality of skeletal morphology
Abnormality of skeletal morphology
1 0 1 0.11 0 0
CUI: C4024854
Disease: Irregular hyperpigmentation of back
Irregular hyperpigmentation of back
1 0 1 0.11 0 0
CUI: C4225259
Disease: SMITH-KINGSMORE SYNDROME
SMITH-KINGSMORE SYNDROME
1 0 1 0.11 0 0
Increased susceptibility to malignancy
1 0 1 0.11 0 0
CUI: C4287832
Disease: Metastatic Malignant Solid Neoplasm
Metastatic Malignant Solid Neoplasm
1 0 1 0.11 0 0
CUI: C4288091
Disease: Tubulocystic renal cell carcinoma
Tubulocystic renal cell carcinoma
1 0 1 0.11 0 0
CUI: C4476709
Disease: Delayed ability to stand
Delayed ability to stand
1 0 1 0.11 0 0
FOCAL CORTICAL DYSPLASIA, TYPE II, SOMATIC
1 0 1 0.11 0 0
CUI: C4525220
Disease: Feline Fibrosarcoma
Feline Fibrosarcoma
1 0 1 0.11 0 0