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: C0233623
Disease: Onychotillomania
Onychotillomania 		1 0 1 8.3E-02 0 0
CUI: C0574763
Disease: Hair absent (finding)
Hair absent (finding) 		1 0 1 8.3E-02 0 0
CUI: C0752288
Disease: Adjustment Sleep Disorder
Adjustment Sleep Disorder 		1 0 1 8.3E-02 0 0
CUI: C0752289
Disease: Environmental Sleep Disorder
Environmental Sleep Disorder 		1 0 1 8.3E-02 0 0
CUI: C0752291
Disease: Limit-Setting Sleep Disorder
Limit-Setting Sleep Disorder 		1 0 1 8.3E-02 0 0
CUI: C0752292
Disease: Nocturnal Eating-Drinking Syndrome
Nocturnal Eating-Drinking Syndrome 		1 0 1 8.3E-02 0 0
CUI: C0752293
Disease: Sleep Disorders, Extrinsic
Sleep Disorders, Extrinsic 		1 0 1 8.3E-02 0 0
CUI: C1844615
Disease: Skin peeling/scaling (newborn)
Skin peeling/scaling (newborn) 		1 0 1 8.3E-02 0 0
CUI: C1844617
Disease: Hypoplastic-absent sebaceous glands
Hypoplastic-absent sebaceous glands 		1 0 1 8.3E-02 0 0
CUI: C1856476
Disease: Gaucher Disease, Type Iiic
Gaucher Disease, Type Iiic 		1 0 1 8.3E-02 0 0
CUI: C1856478
Disease: Hypometric horizontal saccades
Hypometric horizontal saccades 		1 0 1 8.3E-02 0 0
CUI: C1970757
Disease: Tooth Agenesis, Selective, X-Linked, 1
Tooth Agenesis, Selective, X-Linked, 1 		1 0 1 8.3E-02 0 0
CUI: C2129647
Disease: menstrual symptoms
menstrual symptoms 		1 0 1 8.3E-02 0 0
CUI: C2675460
Disease: HAIR MORPHOLOGY 1
HAIR MORPHOLOGY 1 		1 0 1 8.3E-02 0 0
CUI: C2676021
Disease: DEMENTIA, LEWY BODY, SUSCEPTIBILITY TO
DEMENTIA, LEWY BODY, SUSCEPTIBILITY TO 		1 0 1 8.3E-02 0 0
CUI: C2931428
Disease: Hypodontia, X-linked
Hypodontia, X-linked 		1 0 1 8.3E-02 0 0
CUI: C2931585
Disease: Gaucher-like disease
Gaucher-like disease 		1 0 1 8.3E-02 0 0
CUI: C3551587
Disease: ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT 		1 0 1 8.3E-02 0 0
CUI: C3661485
Disease: 17p11.2 Monosomy
17p11.2 Monosomy 		1 0 1 8.3E-02 0 0
CUI: C4021203
Disease: Agenesis of molar
Agenesis of molar 		1 0 1 8.3E-02 0 0
CUI: C4023493
Disease: Beta-EEG
Beta-EEG 		1 0 1 8.3E-02 0 0
CUI: C4023494
Disease: Alpha-EEG
Alpha-EEG 		1 0 1 8.3E-02 0 0
CUI: C4023750
Disease: Aplasia of the maxilla
Aplasia of the maxilla 		1 0 1 8.3E-02 0 0
CUI: C4225255
Disease: YUAN-HAREL-LUPSKI SYNDROME
YUAN-HAREL-LUPSKI SYNDROME 		1 0 1 8.3E-02 0 0
CUI: C4310894
Disease: ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT 		1 0 1 8.3E-02 0 0