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: C4693824
Disease: VERVERI-BRADY SYNDROME
VERVERI-BRADY SYNDROME 		1 5 1 1.0E-01 1 0.14
CUI: C4703584
Disease: Optic ataxia
Optic ataxia 		1 0 1 1.0E-01 0 0
CUI: C2931356
Disease: Spastic paraplegia type 5A, recessive
Spastic paraplegia type 5A, recessive 		13 0 2 9.5E-02 0 0
CUI: C0234512
Disease: Prosopagnosia
Prosopagnosia 		2 0 1 9.1E-02 0 0
CUI: C0263006
Disease: Perifolliculitis
Perifolliculitis 		2 0 1 9.1E-02 0 0
CUI: C0268354
Disease: De Barsy syndrome
De Barsy syndrome 		2 0 1 9.1E-02 0 0
CUI: C0392477
Disease: Congenital flat foot
Congenital flat foot 		2 0 1 9.1E-02 0 0
CUI: C0422895
Disease: Primitive reflex
Primitive reflex 		14 0 2 9.1E-02 0 0
CUI: C1112321
Disease: Congenital cutis laxa
Congenital cutis laxa 		2 0 1 9.1E-02 0 0
CUI: C1838319
Disease: Primitive reflexes (palmomental, snout, glabellar)
Primitive reflexes (palmomental, snout, glabellar) 		14 0 2 9.1E-02 0 0
CUI: C1840404
Disease: Hyperostosis Cranialis Interna
Hyperostosis Cranialis Interna 		2 0 1 9.1E-02 0 0
CUI: C1849115
Disease: SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (disorder)
SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (disorder) 		2 0 1 9.1E-02 0 0
CUI: C1859828
Disease: Increased extraneuronal autofluorescent lipopigment
Increased extraneuronal autofluorescent lipopigment 		2 0 1 9.1E-02 0 0
CUI: C1969722
Disease: Impaired pursuit initiation and maintenance
Impaired pursuit initiation and maintenance 		2 0 1 9.1E-02 0 0
CUI: C2750786
Disease: Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency
Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency 		2 0 1 9.1E-02 0 0
CUI: C2751987
Disease: Cutis Laxa, Autosomal Recessive, Type IIB
Cutis Laxa, Autosomal Recessive, Type IIB 		2 0 1 9.1E-02 0 0
CUI: C3150654
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 84A
DEAFNESS, AUTOSOMAL RECESSIVE 84A 		2 0 1 9.1E-02 0 0
CUI: C3542022
Disease: SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS SYNDROME
SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS SYNDROME 		2 0 1 9.1E-02 0 0
CUI: C3553330
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7 		2 0 1 9.1E-02 0 0
CUI: C3809008
Disease: HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEG SPASTICITY
HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEG SPASTICITY 		2 0 1 9.1E-02 0 0
CUI: C4015095
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 		2 0 1 9.1E-02 0 0
CUI: C4280804
Disease: Percussion-induced rapid rolling muscle contractions
Percussion-induced rapid rolling muscle contractions 		2 0 1 9.1E-02 0 0
CUI: C4476943
Disease: Impaired continence
Impaired continence 		2 0 1 9.1E-02 0 0
CUI: C1849134
Disease: Impaired vibration sensation in the lower limbs
Impaired vibration sensation in the lower limbs 		39 4 4 8.9E-02 1 0.17
CUI: C0022797
Disease: Adult Neuronal Ceroid Lipofuscinosis
Adult Neuronal Ceroid Lipofuscinosis 		16 0 2 8.3E-02 0 0