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: C0265331
Disease: Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder)
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) 		4 0 4 0.20 0 0
CUI: C0242567
Disease: Opsoclonus
Opsoclonus 		5 0 4 0.19 0 0
CUI: C0271344
Disease: Compression of optic nerve
Compression of optic nerve 		8 0 4 0.17 0 0
CUI: C4023722
Disease: Abnormality of hair texture
Abnormality of hair texture 		15 0 5 0.17 0 0
CUI: C3541517
Disease: ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT 		18 0 5 0.15 0 0
CUI: C3888065
Disease: ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT 		18 0 5 0.15 0 0
CUI: C1855642
Disease: Atrophy of alveolar ridges
Atrophy of alveolar ridges 		3 0 3 0.15 0 0
CUI: C0406702
Disease: Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive 		4 0 3 0.14 0 0
CUI: C1318518
Disease: Infantile malignant osteopetrosis
Infantile malignant osteopetrosis 		13 0 4 0.14 0 0
CUI: C0017572
Disease: Gingival Recession
Gingival Recession 		14 0 4 0.13 0 0
CUI: C0235357
Disease: Hypoplasia of teeth
Hypoplasia of teeth 		14 0 4 0.13 0 0
CUI: C0008711
Disease: Chronic rhinitis
Chronic rhinitis 		15 0 4 0.13 0 0
CUI: C4272578
Disease: Autosomal Recessive Osteopetrosis
Autosomal Recessive Osteopetrosis 		24 0 5 0.13 0 0
CUI: C0232513
Disease: Premature tooth loss
Premature tooth loss 		25 0 5 0.12 0 0
CUI: C3539920
Disease: ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE 		25 0 5 0.12 0 0
CUI: C3887494
Disease: ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE 		25 0 5 0.12 0 0
CUI: C1832160
Disease: Abnormality of temperature regulation
Abnormality of temperature regulation 		19 0 4 0.11 0 0
CUI: C0040427
Disease: Tooth Abnormalities
Tooth Abnormalities 		54 0 7 0.10 0 0
CUI: C1290511
Disease: Anodontia of Permanent Dentition
Anodontia of Permanent Dentition 		12 0 3 0.10 0 0
CUI: C0268347
Disease: Ehlers-Danlos Syndrome, Type VIII
Ehlers-Danlos Syndrome, Type VIII 		2 0 2 1.0E-01 0 0
CUI: C1720965
Disease: Ectodermal Dysplasia 3, Anhidrotic
Ectodermal Dysplasia 3, Anhidrotic 		2 0 2 1.0E-01 0 0
CUI: C4022717
Disease: Narrow nasal base
Narrow nasal base 		2 0 2 1.0E-01 0 0
CUI: C4023557
Disease: Abnormality of dental structure
Abnormality of dental structure 		2 0 2 1.0E-01 0 0
CUI: C4024048
Disease: Aplasia of the distal phalanx of the hallux
Aplasia of the distal phalanx of the hallux 		2 0 2 1.0E-01 0 0
CUI: C4024076
Disease: Aplasia/hypoplasia of the 1st metatarsal
Aplasia/hypoplasia of the 1st metatarsal 		2 0 2 1.0E-01 0 0