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: C2673482
Disease: Increased susceptibility to schizophrenia
Increased susceptibility to schizophrenia 		1 0 1 0.50 0 0
CUI: C2675191
Disease: Polymicrogyria, Bilateral Occipital
Polymicrogyria, Bilateral Occipital 		1 0 1 0.50 0 0
CUI: C2675491
Disease: AMYOTROPHIC LATERAL SCLEROSIS 11
AMYOTROPHIC LATERAL SCLEROSIS 11 		1 0 1 0.50 0 0
CUI: C4013648
Disease: POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL
POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL 		1 0 1 0.50 0 0
CUI: C4016483
Disease: PELIZAEUS-MERZBACHER DISEASE, CONNATAL
PELIZAEUS-MERZBACHER DISEASE, CONNATAL 		1 0 1 0.50 0 0
CUI: C4016484
Disease: PELIZAEUS-MERZBACHER DISEASE, MILD
PELIZAEUS-MERZBACHER DISEASE, MILD 		1 0 1 0.50 0 0
CUI: C4021852
Disease: Reduction of oligodendroglia
Reduction of oligodendroglia 		1 0 1 0.50 0 0
CUI: C0751914
Disease: Adult Pelizaeus-Merzbacher Disease
Adult Pelizaeus-Merzbacher Disease 		2 0 1 0.33 0 0
CUI: C0751915
Disease: Pelizaeus-Merzbacher Disease, Atypical
Pelizaeus-Merzbacher Disease, Atypical 		2 0 1 0.33 0 0
CUI: C0751916
Disease: Classic Pelizaeus-Merzbacher Disease
Classic Pelizaeus-Merzbacher Disease 		2 0 1 0.33 0 0
CUI: C0751917
Disease: Pelizaeus-Merzbacher Disease, Transitional
Pelizaeus-Merzbacher Disease, Transitional 		2 0 1 0.33 0 0
CUI: C0751918
Disease: Cockayne-Pelizaeus-Merzbacher Disease
Cockayne-Pelizaeus-Merzbacher Disease 		2 0 1 0.33 0 0
CUI: C1836213
Disease: Aplasia/Hypoplasia of the hallux
Aplasia/Hypoplasia of the hallux 		2 0 1 0.33 0 0
CUI: C3553831
Disease: MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES
MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES 		2 0 1 0.33 0 0
CUI: C4022717
Disease: Narrow nasal base
Narrow nasal base 		2 0 1 0.33 0 0
CUI: C4023557
Disease: Abnormality of dental structure
Abnormality of dental structure 		2 0 1 0.33 0 0
CUI: C4024048
Disease: Aplasia of the distal phalanx of the hallux
Aplasia of the distal phalanx of the hallux 		2 0 1 0.33 0 0
CUI: C4024076
Disease: Aplasia/hypoplasia of the 1st metatarsal
Aplasia/hypoplasia of the 1st metatarsal 		2 0 1 0.33 0 0
CUI: C4024173
Disease: Aplasia of the distal phalanges of the hand
Aplasia of the distal phalanges of the hand 		2 0 1 0.33 0 0
CUI: C4024991
Disease: Aplasia/Hypoplasia of the scapulae
Aplasia/Hypoplasia of the scapulae 		2 0 1 0.33 0 0
CUI: C1857663
Disease: Yunis Varon syndrome
Yunis Varon syndrome 		3 0 1 0.25 0 0
CUI: C1862159
Disease: Short proximal phalanx of hallux
Short proximal phalanx of hallux 		3 0 1 0.25 0 0
CUI: C1970011
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J 		3 0 1 0.25 0 0
CUI: C2675547
Disease: Slender long bones with narrow diaphyses
Slender long bones with narrow diaphyses 		3 0 1 0.25 0 0
CUI: C4022432
Disease: Bilateral external ear deformity
Bilateral external ear deformity 		3 0 1 0.25 0 0