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: C1334439
Disease: adenoid cystic carcinoma of lung
adenoid cystic carcinoma of lung 		1 0 1 2.4E-02 0 0
CUI: C1334963
Disease: Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma
Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma 		1 0 1 2.4E-02 0 0
CUI: C1368295
Disease: Malignant basal cell tumor
Malignant basal cell tumor 		1 0 1 2.4E-02 0 0
CUI: C1834038
Disease: Schilbach-Rott Syndrome
Schilbach-Rott Syndrome 		1 0 1 2.4E-02 0 0
CUI: C1834930
Disease: Fusion of the left and right thalami
Fusion of the left and right thalami 		1 0 1 2.4E-02 0 0
CUI: C1835820
Disease: HOLOPROSENCEPHALY 7
HOLOPROSENCEPHALY 7 		1 0 1 2.4E-02 0 0
CUI: C1835896
Disease: SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE (disorder)
SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE (disorder) 		1 0 1 2.4E-02 0 0
CUI: C1836121
Disease: Al-Gazali Syndrome
Al-Gazali Syndrome 		1 0 1 2.4E-02 0 0
CUI: C1838492
Disease: SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE (disorder)
SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE (disorder) 		1 0 1 2.4E-02 0 0
CUI: C1839727
Disease: Mental Retardation with Spastic Paraplegia
Mental Retardation with Spastic Paraplegia 		1 0 1 2.4E-02 0 0
CUI: C1841686
Disease: Absent hallux
Absent hallux 		1 0 1 2.4E-02 0 0
CUI: C1847406
Disease: Digital Arthropathy-Brachydactyly, Familial
Digital Arthropathy-Brachydactyly, Familial 		1 0 1 2.4E-02 0 0
CUI: C1847408
Disease: Brachytelomesophalangy
Brachytelomesophalangy 		1 0 1 2.4E-02 0 0
CUI: C1847593
Disease: EPIPHYSEAL DYSPLASIA, MULTIPLE, 4
EPIPHYSEAL DYSPLASIA, MULTIPLE, 4 		1 0 1 2.4E-02 0 0
CUI: C1847886
Disease: Anomalous branches of internal carotid artery
Anomalous branches of internal carotid artery 		1 1 1 2.4E-02 1 0.33
CUI: C1848735
Disease: Developmental delay, mild
Developmental delay, mild 		1 0 1 2.4E-02 0 0
CUI: C1849011
Disease: SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE
SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE 		1 0 1 2.4E-02 0 0
CUI: C1849185
Disease: Elevated 7-dehydrocholesterol
Elevated 7-dehydrocholesterol 		1 0 1 2.4E-02 0 0
CUI: C1850190
Disease: Superiorly displaced ears
Superiorly displaced ears 		1 0 1 2.4E-02 0 0
CUI: C1850555
Disease: De La Chapelle Dysplasia
De La Chapelle Dysplasia 		1 0 1 2.4E-02 0 0
CUI: C1851087
Disease: Agenesis of the anterior commissure
Agenesis of the anterior commissure 		1 0 1 2.4E-02 0 0
CUI: C1854749
Disease: Proximal tapering of metacarpals
Proximal tapering of metacarpals 		1 0 1 2.4E-02 0 0
CUI: C1855003
Disease: Bilateral postaxial polydactyly
Bilateral postaxial polydactyly 		1 0 1 2.4E-02 0 0
CUI: C1855305
Disease: Ter Haar syndrome
Ter Haar syndrome 		1 0 1 2.4E-02 0 0
CUI: C1856923
Disease: Double-layered patella
Double-layered patella 		1 0 1 2.4E-02 0 0