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: C0262475
Disease: Congenital abnormality of Eustachian tube
Congenital abnormality of Eustachian tube 		4 0 2 0.29 0 0
CUI: C1298692
Disease: Cleft lip and alveolus
Cleft lip and alveolus 		4 0 2 0.29 0 0
CUI: C4023357
Disease: Maternal teratogenic exposure
Maternal teratogenic exposure 		5 0 2 0.25 0 0
CUI: C4025062
Disease: Supernumerary maxillary incisor
Supernumerary maxillary incisor 		5 0 2 0.25 0 0
CUI: C4025215
Disease: Disturbance of facial expression
Disturbance of facial expression 		5 0 2 0.25 0 0
CUI: C4316811
Disease: Abnormality of the nasal septum
Abnormality of the nasal septum 		5 0 2 0.25 0 0
CUI: C4025060
Disease: Peg-shaped maxillary lateral incisors
Peg-shaped maxillary lateral incisors 		11 0 3 0.23 0 0
CUI: C0158651
Disease: Cleft lip, unilateral, complete
Cleft lip, unilateral, complete 		1 0 1 0.20 0 0
CUI: C0751445
Disease: Encephalitis, Polio
Encephalitis, Polio 		1 0 1 0.20 0 0
CUI: C0751446
Disease: Poliomyelitis, Nonpoliovirus
Poliomyelitis, Nonpoliovirus 		1 0 1 0.20 0 0
CUI: C0751447
Disease: Poliomyelitis, Preparalytic
Poliomyelitis, Preparalytic 		1 0 1 0.20 0 0
CUI: C0796093
Disease: Odontoonychodermal dysplasia
Odontoonychodermal dysplasia 		1 0 1 0.20 0 0
CUI: C1275074
Disease: Odonto-onycho-dermal dysplasia
Odonto-onycho-dermal dysplasia 		1 0 1 0.20 0 0
CUI: C1527258
Disease: Infantile paralysis
Infantile paralysis 		1 0 1 0.20 0 0
CUI: C1704335
Disease: Apocrine cystadenoma
Apocrine cystadenoma 		1 0 1 0.20 0 0
CUI: C1833538
Disease: OROFACIAL CLEFT 7
OROFACIAL CLEFT 7 		1 1 1 0.20 1 0.25
CUI: C1835492
Disease: TOOTH AGENESIS, SELECTIVE, 4 (disorder)
TOOTH AGENESIS, SELECTIVE, 4 (disorder) 		1 0 1 0.20 0 0
CUI: C1835493
Disease: Succedaneous Teeth, Agenesis Of
Succedaneous Teeth, Agenesis Of 		1 0 1 0.20 0 0
CUI: C1837213
Disease: OROFACIAL CLEFT 6, SUSCEPTIBILITY TO
OROFACIAL CLEFT 6, SUSCEPTIBILITY TO 		1 0 1 0.20 0 0
CUI: C1837640
Disease: Deafness, Autosomal Dominant 28
Deafness, Autosomal Dominant 28 		1 0 1 0.20 0 0
CUI: C1857048
Disease: Progressive hypotrichosis
Progressive hypotrichosis 		1 0 1 0.20 0 0
CUI: C1857069
Disease: SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder)
SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder) 		1 0 1 0.20 0 0
CUI: C3841283
Disease: Cleft Palate alone
Cleft Palate alone 		1 0 1 0.20 0 0
CUI: C3873370
Disease: Primary papillary adenocarcinoma of lung
Primary papillary adenocarcinoma of lung 		1 0 1 0.20 0 0
CUI: C4014987
Disease: Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome
Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome 		1 0 1 0.20 0 0