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: C0264955
Disease: Idiopathic arterial calcification of infancy
Idiopathic arterial calcification of infancy 		1 0 1 0.17 0 0
CUI: C1334439
Disease: adenoid cystic carcinoma of lung
adenoid cystic carcinoma of lung 		1 0 1 0.17 0 0
CUI: C1334963
Disease: Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma
Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma 		1 0 1 0.17 0 0
CUI: C1368295
Disease: Malignant basal cell tumor
Malignant basal cell tumor 		1 0 1 0.17 0 0
CUI: C1834038
Disease: Schilbach-Rott Syndrome
Schilbach-Rott Syndrome 		1 0 1 0.17 0 0
CUI: C1834930
Disease: Fusion of the left and right thalami
Fusion of the left and right thalami 		1 0 1 0.17 0 0
CUI: C1835101
Disease: Wide tufts of distal phalanges
Wide tufts of distal phalanges 		1 0 1 0.17 0 0
CUI: C1835820
Disease: HOLOPROSENCEPHALY 7
HOLOPROSENCEPHALY 7 		1 0 1 0.17 0 0
CUI: C1847886
Disease: Anomalous branches of internal carotid artery
Anomalous branches of internal carotid artery 		1 0 1 0.17 0 0
CUI: C1849011
Disease: SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE
SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE 		1 0 1 0.17 0 0
CUI: C1856778
Disease: Widely patent coronal suture
Widely patent coronal suture 		1 0 1 0.17 0 0
CUI: C1867451
Disease: Pseudoxanthoma Elasticum, Heterozygous
Pseudoxanthoma Elasticum, Heterozygous 		1 0 1 0.17 0 0
CUI: C1867453
Disease: Peau d'orange retinal changes
Peau d'orange retinal changes 		1 0 1 0.17 0 0
CUI: C1968577
Disease: Progressive calcification of costochondral cartilage
Progressive calcification of costochondral cartilage 		1 0 1 0.17 0 0
CUI: C2033396
Disease: Yellow papule
Yellow papule 		1 0 1 0.17 0 0
CUI: C3276161
Disease: ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2
ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2 		1 0 1 0.17 0 0
CUI: C3278138
Disease: FIBROCHONDROGENESIS 1
FIBROCHONDROGENESIS 1 		1 0 1 0.17 0 0
CUI: C3711390
Disease: 9q22.3 Microdeletion
9q22.3 Microdeletion 		1 0 1 0.17 0 0
CUI: C3805371
Disease: Pits of palms and soles
Pits of palms and soles 		1 0 1 0.17 0 0
CUI: C4015965
Disease: MARSHALL/STICKLER SYNDROME
MARSHALL/STICKLER SYNDROME 		1 0 1 0.17 0 0
CUI: C4022181
Disease: Meningeal calcification
Meningeal calcification 		1 0 1 0.17 0 0
CUI: C4022895
Disease: Medial calcification of medium-sized arteries
Medial calcification of medium-sized arteries 		1 0 1 0.17 0 0
CUI: C4022969
Disease: Small proximal tibial epiphyses
Small proximal tibial epiphyses 		1 0 1 0.17 0 0
CUI: C4022970
Disease: Small distal femoral epiphysis
Small distal femoral epiphysis 		1 0 1 0.17 0 0
CUI: C4023930
Disease: Enlarged epiphyses of the proximal phalanges of the hand
Enlarged epiphyses of the proximal phalanges of the hand 		1 0 1 0.17 0 0