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: C0001145
Disease: Acne Keloid
Acne Keloid 		1 0 1 0.25 0 0
CUI: C0040072
Disease: Thymic Cyst
Thymic Cyst 		1 0 1 0.25 0 0
CUI: C0406344
Disease: Follicular ichthyosis
Follicular ichthyosis 		1 0 1 0.25 0 0
CUI: C0424000
Disease: Feeling suicidal (finding)
Feeling suicidal (finding) 		1 0 1 0.25 0 0
CUI: C1832817
Disease: Klippel-Feil deformity, conductive deafness, and absent vagina
Klippel-Feil deformity, conductive deafness, and absent vagina 		1 0 1 0.25 0 0
CUI: C1845576
Disease: Unilateral chest hypoplasia
Unilateral chest hypoplasia 		1 0 1 0.25 0 0
CUI: C2748531
Disease: Perifollicular fibrosis
Perifollicular fibrosis 		1 0 1 0.25 0 0
CUI: C3502469
Disease: Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia
Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia 		1 0 1 0.25 0 0
CUI: C3806745
Disease: PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES, X-LINKED
PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES, X-LINKED 		1 0 1 0.25 0 0
CUI: C4016470
Disease: IFAP SYNDROME
IFAP SYNDROME 		1 0 1 0.25 0 0
CUI: C4540040
Disease: FRASER SYNDROME 3
FRASER SYNDROME 3 		1 0 1 0.25 0 0
CUI: C4746956
Disease: OSTEOGENESIS IMPERFECTA, TYPE XIX
OSTEOGENESIS IMPERFECTA, TYPE XIX 		1 0 1 0.25 0 0
CUI: C0240444
Disease: Pachyonychia
Pachyonychia 		2 0 1 0.20 0 0
CUI: C0266273
Disease: Congenital absence of adrenal gland
Congenital absence of adrenal gland 		2 0 1 0.20 0 0
CUI: C1275091
Disease: Ichthyosis follicularis with alopecia and photophobia (IFAP)
Ichthyosis follicularis with alopecia and photophobia (IFAP) 		2 0 1 0.20 0 0
CUI: C1841990
Disease: Aplasia of the vagina
Aplasia of the vagina 		2 0 1 0.20 0 0
CUI: C1854260
Disease: LEBER CONGENITAL AMAUROSIS 6 (disorder)
LEBER CONGENITAL AMAUROSIS 6 (disorder) 		2 0 1 0.20 0 0
CUI: C2673873
Disease: BARDET-BIEDL SYNDROME 13
BARDET-BIEDL SYNDROME 13 		2 0 1 0.20 0 0
CUI: C2678492
Disease: Sex Reversal, Female, With Dysgenesis Of Kidneys, Adrenals, And Lungs
Sex Reversal, Female, With Dysgenesis Of Kidneys, Adrenals, And Lungs 		2 0 1 0.20 0 0
CUI: C2713583
Disease: Congenital Tracheobronchomegaly
Congenital Tracheobronchomegaly 		2 0 1 0.20 0 0
CUI: C3887525
Disease: Keratosis Follicularis Spinulosa Decalvans, X-Linked
Keratosis Follicularis Spinulosa Decalvans, X-Linked 		2 0 1 0.20 0 0
CUI: C4022750
Disease: Thin fingernail
Thin fingernail 		2 0 1 0.20 0 0
CUI: C4024646
Disease: Aplasia/Hypoplasia of the fallopian tube
Aplasia/Hypoplasia of the fallopian tube 		2 0 1 0.20 0 0
CUI: C4310705
Disease: JOUBERT SYNDROME 28
JOUBERT SYNDROME 28 		2 0 1 0.20 0 0
CUI: C0221245
Disease: Fissure in skin
Fissure in skin 		3 0 1 0.17 0 0