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: C4025644
Disease: Hypothalamic gonadotropin-releasing hormone deficiency
Hypothalamic gonadotropin-releasing hormone deficiency 		22 0 22 0.20 0 0
CUI: C4022003
Disease: Erectile abnormalities
Erectile abnormalities 		24 0 22 0.20 0 0
CUI: C0266013
Disease: Congenital hypoplasia of breast
Congenital hypoplasia of breast 		38 0 23 0.18 0 0
CUI: C0542519
Disease: Congenital absence of kidney
Congenital absence of kidney 		33 0 22 0.18 0 0
CUI: C0003126
Disease: Anosmia
Anosmia 		40 0 23 0.18 0 0
CUI: C4024202
Disease: Reduced number of teeth
Reduced number of teeth 		67 0 27 0.18 0 0
CUI: C4025821
Disease: Anterior hypopituitarism
Anterior hypopituitarism 		48 0 24 0.18 0 0
CUI: C1619700
Disease: RENAL ADYSPLASIA
RENAL ADYSPLASIA 		29 0 21 0.18 0 0
CUI: C2674432
Disease: Reduced bone mineral density
Reduced bone mineral density 		76 0 28 0.18 0 0
CUI: C1384606
Disease: Dyspareunia
Dyspareunia 		37 0 22 0.18 0 0
CUI: C0008297
Disease: Choanal Atresia
Choanal Atresia 		104 0 32 0.18 0 0
CUI: C4049796
Disease: Abnormality of cardiovascular system morphology
Abnormality of cardiovascular system morphology 		198 0 46 0.18 0 0
CUI: C0454455
Disease: Mirror movements disorder
Mirror movements disorder 		39 0 22 0.17 0 0
CUI: C0520927
Disease: Decreased fertility
Decreased fertility 		50 0 23 0.17 0 0
CUI: C0266174
Disease: Duodenal atresia
Duodenal atresia 		39 0 21 0.16 0 0
CUI: C0266362
Disease: Ambiguous Genitalia
Ambiguous Genitalia 		109 0 30 0.16 0 0
CUI: C0030486
Disease: Paraplegia
Paraplegia 		59 0 23 0.16 0 0
CUI: C2364082
Disease: Sense of smell impaired
Sense of smell impaired 		60 0 23 0.16 0 0
CUI: C4021776
Disease: Abnormality of the voice
Abnormality of the voice 		64 0 23 0.15 0 0
CUI: C0242343
Disease: Panhypopituitarism
Panhypopituitarism 		73 0 24 0.15 0 0
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly 		37 0 19 0.15 0 0
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		86 0 25 0.15 0 0
CUI: C1840238
Disease: Midnasal stenosis
Midnasal stenosis 		16 0 16 0.15 0 0
CUI: C0241355
Disease: Small testicle
Small testicle 		129 0 30 0.14 0 0
CUI: C1840235
Disease: SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR
SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR 		20 0 16 0.14 0 0