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: C3887525
Disease: Keratosis Follicularis Spinulosa Decalvans, X-Linked
Keratosis Follicularis Spinulosa Decalvans, X-Linked 		2 1 2 0.50 1 1.00
CUI: C0268418
Disease: Deficiency of glycerol kinase
Deficiency of glycerol kinase 		3 0 2 0.40 0 0
CUI: C0343057
Disease: Keratosis pilaris decalvans
Keratosis pilaris decalvans 		3 0 2 0.40 0 0
CUI: C1839988
Disease: Ichthyosis follicularis atrichia photophobia syndrome
Ichthyosis follicularis atrichia photophobia syndrome 		3 0 2 0.40 0 0
CUI: C2609071
Disease: Olmsted syndrome
Olmsted syndrome 		5 0 2 0.29 0 0
CUI: C0001145
Disease: Acne Keloid
Acne Keloid 		1 0 1 0.25 0 0
CUI: C0001529
Disease: Adiposis Dolorosa
Adiposis Dolorosa 		1 0 1 0.25 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 0.25 0 0
CUI: C0406344
Disease: Follicular ichthyosis
Follicular ichthyosis 		1 0 1 0.25 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 0.25 0 0
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		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: C2875313
Disease: Severe [Duchenne] muscular dystrophy
Severe [Duchenne] muscular dystrophy 		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: C3844818
Disease: Attention Deficit Hyper Activity
Attention Deficit Hyper Activity 		1 0 1 0.25 0 0
CUI: C4016470
Disease: IFAP SYNDROME
IFAP SYNDROME 		1 0 1 0.25 0 0
CUI: C4016476
Disease: DUCHENNE MUSCULAR DYSTROPHY, MENTAL RETARDATION, AND ABSENCE OF ERG B-WAVE
DUCHENNE MUSCULAR DYSTROPHY, MENTAL RETARDATION, AND ABSENCE OF ERG B-WAVE 		1 0 1 0.25 0 0
CUI: C4016477
Disease: INTERMEDIATE MUSCULAR DYSTROPHY
INTERMEDIATE MUSCULAR DYSTROPHY 		1 0 1 0.25 0 0
CUI: C4022648
Disease: Abnormal muscle fiber dystrophin expression
Abnormal muscle fiber dystrophin expression 		1 0 1 0.25 0 0
CUI: C4505291
Disease: Xp21 Contiguous Gene Deletion Syndrome
Xp21 Contiguous Gene Deletion Syndrome 		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: C0026851
Disease: Muscular Dystrophy, Animal
Muscular Dystrophy, Animal 		2 0 1 0.20 0 0
CUI: C0039223
Disease: Tabes Dorsalis
Tabes Dorsalis 		2 0 1 0.20 0 0