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: C3552553
Disease: HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA
HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA 		1 0 1 0.12 0 0
CUI: C4021794
Disease: Abnormality of the adrenal glands
Abnormality of the adrenal glands 		10 0 2 0.12 0 0
CUI: C4021943
Disease: Abnormality of the xiphoid process
Abnormality of the xiphoid process 		1 0 1 0.12 0 0
CUI: C4073246
Disease: Abnormal cricoid cartilage morphology
Abnormal cricoid cartilage morphology 		1 0 1 0.12 0 0
CUI: C4280276
Disease: Cleft alveolar process of maxilla
Cleft alveolar process of maxilla 		1 0 1 0.12 0 0
CUI: C4476590
Disease: Abnormal morphology of the hippocampus
Abnormal morphology of the hippocampus 		1 0 1 0.12 0 0
CUI: C4693651
Disease: OROFACIODIGITAL SYNDROME XVIII
OROFACIODIGITAL SYNDROME XVIII 		1 0 1 0.12 0 0
CUI: C4748219
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65 		1 0 1 0.12 0 0
CUI: C0158779
Disease: Cervical rib
Cervical rib 		11 0 2 0.12 0 0
CUI: C1851792
Disease: Aplasia/Hypoplasia of the earlobes
Aplasia/Hypoplasia of the earlobes 		11 0 2 0.12 0 0
CUI: C1504382
Disease: Pulmonary arterial medial hypertrophy
Pulmonary arterial medial hypertrophy 		2 0 1 0.11 0 0
CUI: C1836868
Disease: Broad ischia
Broad ischia 		2 0 1 0.11 0 0
CUI: C1844862
Disease: Abruzzo Erickson syndrome
Abruzzo Erickson syndrome 		2 0 1 0.11 0 0
CUI: C3810023
Disease: VERHEIJ SYNDROME
VERHEIJ SYNDROME 		2 0 1 0.11 0 0
CUI: C3874334
Disease: Severe hearing loss
Severe hearing loss 		2 0 1 0.11 0 0
CUI: C4023237
Disease: Interrupted inferior vena cava with azygous continuation
Interrupted inferior vena cava with azygous continuation 		2 0 1 0.11 0 0
CUI: C4023411
Disease: Hemifacial hypoplasia
Hemifacial hypoplasia 		2 0 1 0.11 0 0
CUI: C4024831
Disease: Blotching pigmentation of the skin
Blotching pigmentation of the skin 		2 0 1 0.11 0 0
CUI: C4319808
Disease: Trisomy 13 Syndrome
Trisomy 13 Syndrome 		2 0 1 0.11 0 0
CUI: C0152419
Disease: Interrupted aortic arch
Interrupted aortic arch 		13 0 2 0.11 0 0
CUI: C4025663
Disease: Abnormality of tibia morphology
Abnormality of tibia morphology 		13 0 2 0.11 0 0
CUI: C0155964
Disease: Atrophy of tongue papillae
Atrophy of tongue papillae 		3 0 1 1.0E-01 0 0
CUI: C1401781
Disease: Short uvula
Short uvula 		3 0 1 1.0E-01 0 0
CUI: C1832130
Disease: Pursed lips
Pursed lips 		3 0 1 1.0E-01 0 0
CUI: C1861873
Disease: Multiple plantar creases
Multiple plantar creases 		3 0 1 1.0E-01 0 0