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: C0235857
Disease: Decreased lacrimation
Decreased lacrimation 		6 0 1 0.14 0 0
CUI: C0406803
Disease: Syringocystadenoma Papilliferum
Syringocystadenoma Papilliferum 		6 0 1 0.14 0 0
CUI: C0546275
Disease: Hypoganglionosis
Hypoganglionosis 		6 0 1 0.14 0 0
CUI: C1833296
Disease: FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED
FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED 		6 0 1 0.14 0 0
CUI: C1866636
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C 		6 0 1 0.14 0 0
CUI: C0334439
Disease: Malignant desmoplastic melanoma
Malignant desmoplastic melanoma 		7 0 1 0.12 0 0
CUI: C0346027
Disease: Eccrine epithelioma
Eccrine epithelioma 		7 0 1 0.12 0 0
CUI: C0348489
Disease: Other sphingolipidosis
Other sphingolipidosis 		7 0 1 0.12 0 0
CUI: C1836737
Disease: White eyebrow
White eyebrow 		7 0 1 0.12 0 0
CUI: C1855331
Disease: Olfactory lobe agenesis
Olfactory lobe agenesis 		7 0 1 0.12 0 0
CUI: C1860339
Disease: WAARDENBURG SYNDROME, TYPE IIA
WAARDENBURG SYNDROME, TYPE IIA 		7 0 2 0.29 0 0
CUI: C4024927
Disease: Peripheral hypomyelination
Peripheral hypomyelination 		7 0 1 0.12 0 0
CUI: C0205854
Disease: Glandular Neoplasms
Glandular Neoplasms 		8 0 1 0.11 0 0
CUI: C0345244
Disease: Neuronal intestinal dysplasia
Neuronal intestinal dysplasia 		8 0 1 0.11 0 0
CUI: C1260326
Disease: Dendritic Cell Sarcoma, Interdigitating
Dendritic Cell Sarcoma, Interdigitating 		8 0 1 0.11 0 0
CUI: C1836736
Disease: White eyelashes
White eyelashes 		8 0 1 0.11 0 0
CUI: C0025160
Disease: Megacolon
Megacolon 		9 9 2 0.22 1 3.3E-02
CUI: C2700265
Disease: Waardenburg Syndrome Type 2
Waardenburg Syndrome Type 2 		9 0 1 1.0E-01 0 0
CUI: C0334348
Disease: Hidradenoma Papilliferum
Hidradenoma Papilliferum 		10 0 1 9.1E-02 0 0
CUI: C0393808
Disease: Charcot-Marie-Tooth disease, X-linked, 1
Charcot-Marie-Tooth disease, X-linked, 1 		10 0 1 9.1E-02 0 0
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome 		10 0 1 9.1E-02 0 0
CUI: C4274084
Disease: Pelizaeus Merzbacher like disease
Pelizaeus Merzbacher like disease 		10 0 1 9.1E-02 0 0
CUI: C0266200
Disease: Microcolon
Microcolon 		11 0 1 8.3E-02 0 0
CUI: C0393818
Disease: Congenital hypomyelinating neuropathy
Congenital hypomyelinating neuropathy 		11 0 1 8.3E-02 0 0
CUI: C2936419
Disease: 46, XX Testicular Disorders of Sex Development
46, XX Testicular Disorders of Sex Development 		11 0 1 8.3E-02 0 0