Source: ALL
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: C0234022
Disease: Anorgasmia
Anorgasmia 		1 0 1 1.2E-02 0 0
CUI: C0268356
Disease: Osteogenesis imperfecta with blue sclerae AND normal teeth
Osteogenesis imperfecta with blue sclerae AND normal teeth 		1 0 1 1.2E-02 0 0
CUI: C0278776
Disease: recurrent childhood acute myeloid leukemia
recurrent childhood acute myeloid leukemia 		1 0 1 1.2E-02 0 0
CUI: C0741146
Disease: anxiety acute
anxiety acute 		1 0 1 1.2E-02 0 0
CUI: C0795888
Disease: AUTISM, SUSCEPTIBILITY TO, X-LINKED 4
AUTISM, SUSCEPTIBILITY TO, X-LINKED 4 		1 0 1 1.2E-02 0 0
CUI: C1334068
Disease: Hypercellular bone marrow
Hypercellular bone marrow 		1 0 1 1.2E-02 0 0
CUI: C1832733
Disease: Rhabdomyolysis, Cerivastatin-Induced
Rhabdomyolysis, Cerivastatin-Induced 		1 0 1 1.2E-02 0 0
CUI: C1843983
Disease: Trapezoidal distal femoral condyles
Trapezoidal distal femoral condyles 		1 0 1 1.2E-02 0 0
CUI: C1843985
Disease: Shortening of the talar neck
Shortening of the talar neck 		1 0 1 1.2E-02 0 0
CUI: C1843986
Disease: Flattening of the talar dome
Flattening of the talar dome 		1 0 1 1.2E-02 0 0
CUI: C1857034
Disease: Ehlers-Danlos syndrome, cardiac valvular form
Ehlers-Danlos syndrome, cardiac valvular form 		1 0 1 1.2E-02 0 0
CUI: C2677879
Disease: Hypospadias 2, X-Linked
Hypospadias 2, X-Linked 		1 0 1 1.2E-02 0 0
CUI: C3151411
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 6
MENTAL RETARDATION, AUTOSOMAL DOMINANT 6 		1 0 1 1.2E-02 0 0
CUI: C4015316
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27 		1 0 1 1.2E-02 0 0
CUI: C4021839
Disease: Abnormal dense granule content
Abnormal dense granule content 		1 0 1 1.2E-02 0 0
CUI: C4022863
Disease: Abnormal alpha granule content
Abnormal alpha granule content 		1 0 1 1.2E-02 0 0
CUI: C4225221
Disease: RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2
RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2 		1 0 1 1.2E-02 0 0
CUI: C4225222
Disease: TAKENOUCHI-KOSAKI SYNDROME
TAKENOUCHI-KOSAKI SYNDROME 		1 0 1 1.2E-02 0 0
CUI: C4225340
Disease: BRUGADA SYNDROME 9
BRUGADA SYNDROME 9 		1 0 1 1.2E-02 0 0
CUI: C4303789
Disease: Ehlers-Danlos syndrome cardiac valvular type
Ehlers-Danlos syndrome cardiac valvular type 		1 0 1 1.2E-02 0 0
CUI: C4310978
Disease: EHLERS-DANLOS/OSTEOGENESIS IMPERFECTA CROSSOVER SYNDROME
EHLERS-DANLOS/OSTEOGENESIS IMPERFECTA CROSSOVER SYNDROME 		1 0 1 1.2E-02 0 0
CUI: C4693948
Disease: DRUG METABOLISM, ALTERED, CYP2C8-RELATED
DRUG METABOLISM, ALTERED, CYP2C8-RELATED 		1 0 1 1.2E-02 0 0
CUI: C0154733
Disease: Multiple cranial nerve palsy
Multiple cranial nerve palsy 		2 0 1 1.2E-02 0 0
CUI: C0238157
Disease: Benign hematuria
Benign hematuria 		2 0 1 1.2E-02 0 0
CUI: C0266807
Disease: Acute gastrointestinal hemorrhage
Acute gastrointestinal hemorrhage 		2 0 1 1.2E-02 0 0