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: C1335911
Disease: Salivary Gland Sialoblastoma
Salivary Gland Sialoblastoma 		1 0 1 0.25 0 0
CUI: C1861799
Disease: Catatrichy
Catatrichy 		1 0 1 0.25 0 0
CUI: C1866425
Disease: Yemenite deaf-blind hypopigmentation syndrome
Yemenite deaf-blind hypopigmentation syndrome 		1 0 1 0.25 0 0
CUI: C3266028
Disease: Pigmented actinic keratosis
Pigmented actinic keratosis 		1 0 1 0.25 0 0
CUI: C4022600
Disease: Peripheral amyelination
Peripheral amyelination 		1 0 1 0.25 0 0
CUI: C4023430
Disease: Long-segment aganglionic megacolon
Long-segment aganglionic megacolon 		1 0 1 0.25 0 0
CUI: C4025609
Disease: EMG: axonal abnormality
EMG: axonal abnormality 		6 4 2 0.25 2 0.50
CUI: C4073057
Disease: Color vision test abnormality
Color vision test abnormality 		1 0 1 0.25 0 0
CUI: C0268252
Disease: Late-Onset Globoid Cell Leukodystrophy
Late-Onset Globoid Cell Leukodystrophy 		2 0 1 0.20 0 0
CUI: C0334266
Disease: Transitional cell papilloma, benign
Transitional cell papilloma, benign 		2 0 1 0.20 0 0
CUI: C0751273
Disease: Infantile Globoid Cell Leukodystrophy
Infantile Globoid Cell Leukodystrophy 		2 0 1 0.20 0 0
CUI: C1969722
Disease: Impaired pursuit initiation and maintenance
Impaired pursuit initiation and maintenance 		2 0 1 0.20 0 0
CUI: C2673266
Disease: KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY
KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY 		2 0 1 0.20 0 0
CUI: C2750452
Disease: Waardenburg Syndrome, Type 4c
Waardenburg Syndrome, Type 4c 		2 0 1 0.20 0 0
CUI: C3668943
Disease: Fatty Acid Hydroxylase-Associated Neurodegeneration
Fatty Acid Hydroxylase-Associated Neurodegeneration 		2 0 1 0.20 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 0.20 0 0
CUI: C4023373
Disease: Demyelinating sensory neuropathy
Demyelinating sensory neuropathy 		2 0 1 0.20 0 0
CUI: C4023376
Disease: Abnormality of the dorsal column of the spinal cord
Abnormality of the dorsal column of the spinal cord 		2 0 1 0.20 0 0
CUI: C4023381
Disease: Morphological abnormality of the inner ear
Morphological abnormality of the inner ear 		2 0 1 0.20 0 0
CUI: C4023387
Disease: Dilated vestibule of the inner ear
Dilated vestibule of the inner ear 		2 0 1 0.20 0 0
CUI: C4024772
Disease: Abnormal flash visual evoked potentials
Abnormal flash visual evoked potentials 		2 0 1 0.20 0 0
CUI: C0011103
Disease: Decerebrate State
Decerebrate State 		3 0 1 0.17 0 0
CUI: C0206673
Disease: Syringoma
Syringoma 		3 0 1 0.17 0 0
CUI: C1836727
Disease: Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease 		3 0 1 0.17 0 0
CUI: C2700405
Disease: WAARDENBURG SYNDROME, TYPE IIE
WAARDENBURG SYNDROME, TYPE IIE 		3 0 1 0.17 0 0