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: C4303860
Disease: Craniofacial ulnar renal syndrome
Craniofacial ulnar renal syndrome
3 0 3 0.43 0 0
CUI: C0796032
Disease: Malpuech facial clefting syndrome
Malpuech facial clefting syndrome
4 0 3 0.38 0 0
CUI: C3277117
Disease: Caudal appendage
Caudal appendage
6 0 3 0.30 0 0
CUI: C4022490
Disease: Prominent coccyx
Prominent coccyx
6 0 3 0.30 0 0
CUI: C0796059
Disease: Oculopalatoskeletal syndrome
Oculopalatoskeletal syndrome
2 0 2 0.29 0 0
Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia
3 0 2 0.25 0 0
CUI: C1303003
Disease: Epicanthus inversus
Epicanthus inversus
9 0 3 0.23 0 0
CUI: C0796279
Disease: Carnevale syndrome
Carnevale syndrome
4 0 2 0.22 0 0
CUI: C0036305
Disease: Schamberg Disease
Schamberg Disease
6 0 2 0.18 0 0
CUI: C3808403
Disease: Large fleshy ears
Large fleshy ears
13 0 3 0.18 0 0
CUI: C0398639
Disease: Amegakaryocytic thrombocytopenia
Amegakaryocytic thrombocytopenia
7 0 2 0.17 0 0
Congenital amegakaryocytic thrombocytopenia
7 0 2 0.17 0 0
CUI: C2674451
Disease: Anterior radial head dislocation
Anterior radial head dislocation
1 0 1 0.14 0 0
CUI: C2697767
Disease: Interleukin 19 Measurement
Interleukin 19 Measurement
1 0 1 0.14 0 0
CUI: C4022548
Disease: Hyperplastic callus formation
Hyperplastic callus formation
1 0 1 0.14 0 0
CUI: C4025228
Disease: Partial abdominal muscle agenesis
Partial abdominal muscle agenesis
1 0 1 0.14 0 0
RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2
1 0 1 0.14 0 0
Desmin related myopathy with Mallory body-like inclusions
1 0 1 0.14 0 0
RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 1
1 0 1 0.14 0 0
CUI: C3152182
Disease: Anterior chamber anomalies
Anterior chamber anomalies
18 0 3 0.14 0 0
CUI: C0740268
Disease: Pelvic prolapse
Pelvic prolapse
2 0 1 0.12 0 0
Single interphalangeal crease of fifth finger
2 0 1 0.12 0 0
CUI: C1859292
Disease: Triangular-shaped open mouth
Triangular-shaped open mouth
2 3 1 0.12 3 1.00
Type 1 and type 2 muscle fiber minicore regions
2 0 1 0.12 0 0
CUI: C0221766
Disease: Diastasis recti
Diastasis recti
22 0 3 0.12 0 0