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: 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: C4022964
Disease: Abnormality of the occipital bone
Abnormality of the occipital bone 		4 0 2 0.50 0 0
CUI: C4023709
Disease: Sacrococcygeal pilonidal abnormality
Sacrococcygeal pilonidal abnormality 		1 0 1 0.50 0 0
CUI: C4023736
Disease: 2-5 finger syndactyly
2-5 finger syndactyly 		1 0 1 0.50 0 0
CUI: C4024164
Disease: Thin ear helix
Thin ear helix 		1 0 1 0.50 0 0
CUI: C4225499
Disease: MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES
MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES 		1 2 1 0.50 1 0.12
CUI: C0333457
Disease: Segmental demyelination
Segmental demyelination 		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: 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
CUI: C4023731
Disease: 4-5 finger syndactyly
4-5 finger syndactyly 		3 0 1 0.25 0 0
CUI: C4025132
Disease: Shortening of all distal phalanges of the toes
Shortening of all distal phalanges of the toes 		3 0 1 0.25 0 0
CUI: C4025828
Disease: Abnormality of the scapula
Abnormality of the scapula 		3 0 1 0.25 0 0
CUI: C1839276
Disease: Broad secondary alveolar ridge
Broad secondary alveolar ridge 		4 0 1 0.20 0 0