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: C0235198
Disease: Unable to concentrate
Unable to concentrate 		1 1 1 0.25 1 0.33
CUI: C1334963
Disease: Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma
Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma 		1 0 1 0.25 0 0
CUI: C1368295
Disease: Malignant basal cell tumor
Malignant basal cell tumor 		1 0 1 0.25 0 0
CUI: C1834038
Disease: Schilbach-Rott Syndrome
Schilbach-Rott Syndrome 		1 0 1 0.25 0 0
CUI: C1834930
Disease: Fusion of the left and right thalami
Fusion of the left and right thalami 		1 0 1 0.25 0 0
CUI: C1835820
Disease: HOLOPROSENCEPHALY 7
HOLOPROSENCEPHALY 7 		1 0 1 0.25 0 0
CUI: C1847886
Disease: Anomalous branches of internal carotid artery
Anomalous branches of internal carotid artery 		1 1 1 0.25 1 0.33
CUI: C3711390
Disease: 9q22.3 Microdeletion
9q22.3 Microdeletion 		1 0 1 0.25 0 0
CUI: C3805371
Disease: Pits of palms and soles
Pits of palms and soles 		1 0 1 0.25 0 0
CUI: C4022774
Disease: Focal T2 hyperintense thalamic lesion
Focal T2 hyperintense thalamic lesion 		1 1 1 0.25 1 0.33
CUI: C4022968
Disease: Abnormal hypothalamus physiology
Abnormal hypothalamus physiology 		1 1 1 0.25 1 0.33
CUI: C4023808
Disease: Hyperextensibility at elbow
Hyperextensibility at elbow 		11 7 3 0.25 2 0.25
CUI: C4023930
Disease: Enlarged epiphyses of the proximal phalanges of the hand
Enlarged epiphyses of the proximal phalanges of the hand 		1 1 1 0.25 1 0.33
CUI: C4024230
Disease: Contracture of the distal interphalangeal joint of the fingers
Contracture of the distal interphalangeal joint of the fingers 		1 1 1 0.25 1 0.33
CUI: C4025542
Disease: Humeral cortical thickening
Humeral cortical thickening 		1 1 1 0.25 1 0.33
CUI: C4025842
Disease: Abnormal uvea morphology
Abnormal uvea morphology 		1 1 1 0.25 1 0.33
CUI: C4225243
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z 		1 0 1 0.25 0 0
CUI: C4225667
Disease: CHROMOSOME 16p13.2 DELETION SYNDROME
CHROMOSOME 16p13.2 DELETION SYNDROME 		1 0 1 0.25 0 0
CUI: C4476818
Disease: Nevus sebaceus
Nevus sebaceus 		1 0 1 0.25 0 0
CUI: C0334574
Disease: Calcifying Epithelial Odontogenic Tumor
Calcifying Epithelial Odontogenic Tumor 		2 0 1 0.20 0 0
CUI: C1854245
Disease: Basal cell carcinoma, multiple
Basal cell carcinoma, multiple 		2 0 1 0.20 0 0
CUI: C1859376
Disease: Fused sternal ossification centers
Fused sternal ossification centers 		2 1 1 0.20 1 0.33
CUI: C1862314
Disease: Basal cell nevus
Basal cell nevus 		2 0 1 0.20 0 0
CUI: C4020919
Disease: Dense metaphyseal bands
Dense metaphyseal bands 		2 1 1 0.20 1 0.33
CUI: C4021598
Disease: Distal tibial bowing
Distal tibial bowing 		2 1 1 0.20 1 0.33