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: C0270150
Disease: Perinatal respiratory failure
Perinatal respiratory failure 		1 0 1 0.17 0 0
CUI: C1655035
Disease: congenital muscle disorder
congenital muscle disorder 		1 0 1 0.17 0 0
CUI: C1854061
Disease: Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness
Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness 		1 0 1 0.17 0 0
CUI: C1869122
Disease: EHLERS-DANLOS SYNDROME, PROGEROID FORM
EHLERS-DANLOS SYNDROME, PROGEROID FORM 		1 0 1 0.17 0 0
CUI: C4021596
Disease: Abnormality of primary teeth
Abnormality of primary teeth 		1 0 1 0.17 0 0
CUI: C4021601
Disease: Premature eruption of permanent teeth
Premature eruption of permanent teeth 		1 0 1 0.17 0 0
CUI: C4024855
Disease: Lack of subcutaneous fatty tissue
Lack of subcutaneous fatty tissue 		1 0 1 0.17 0 0
CUI: C4540327
Disease: NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES 		1 0 1 0.17 0 0
CUI: C0014536
Disease: Epidural Neoplasms
Epidural Neoplasms 		2 0 1 0.14 0 0
CUI: C1837733
Disease: Broad lateral eyebrow
Broad lateral eyebrow 		2 0 1 0.14 0 0
CUI: C1846169
Disease: Myotubular Myopathy with Abnormal Genital Development
Myotubular Myopathy with Abnormal Genital Development 		2 0 1 0.14 0 0
CUI: C1851797
Disease: Palmoplantar cutis gyrata
Palmoplantar cutis gyrata 		2 0 1 0.14 0 0
CUI: C2931009
Disease: Congenital disorder of glycosylation type 2D
Congenital disorder of glycosylation type 2D 		2 0 1 0.14 0 0
CUI: C4024963
Disease: Abnormal aggressive, impulsive or violent behavior
Abnormal aggressive, impulsive or violent behavior 		2 0 1 0.14 0 0
CUI: C4025139
Disease: Fifth finger distal phalanx clinodactyly
Fifth finger distal phalanx clinodactyly 		2 0 1 0.14 0 0
CUI: C0016399
Disease: Epilepsy, Partial, Motor
Epilepsy, Partial, Motor 		3 0 1 0.12 0 0
CUI: C0234861
Disease: Cri du chat
Cri du chat 		3 0 1 0.12 0 0
CUI: C1335411
Disease: Cyst of pineal gland
Cyst of pineal gland 		3 0 1 0.12 0 0
CUI: C1844734
Disease: Hemihypotrophy of lower limb
Hemihypotrophy of lower limb 		3 0 1 0.12 0 0
CUI: C1848182
Disease: Blind vagina
Blind vagina 		3 0 1 0.12 0 0
CUI: C1858278
Disease: Charcot-Marie-Tooth disease, Type 4B2
Charcot-Marie-Tooth disease, Type 4B2 		3 0 1 0.12 0 0
CUI: C1861325
Disease: Progressive conductive hearing impairment
Progressive conductive hearing impairment 		3 0 1 0.12 0 0
CUI: C3278404
Disease: MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS
MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS 		3 0 1 0.12 0 0
CUI: C4021573
Disease: Patchy hypo- and hyperpigmentation
Patchy hypo- and hyperpigmentation 		3 0 1 0.12 0 0
CUI: C4023408
Disease: Abnormality of mouth size
Abnormality of mouth size 		3 0 1 0.12 0 0