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: C1862863
Disease: Sparse body hair
Sparse body hair 		57 0 18 8.7E-02 0 0
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		86 0 20 8.5E-02 0 0
CUI: C4021776
Disease: Abnormality of the voice
Abnormality of the voice 		64 0 18 8.4E-02 0 0
CUI: C1865866
Disease: Congenital sensorineural hearing loss
Congenital sensorineural hearing loss 		68 0 18 8.3E-02 0 0
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		178 0 26 8.1E-02 0 0
CUI: C4025644
Disease: Hypothalamic gonadotropin-releasing hormone deficiency
Hypothalamic gonadotropin-releasing hormone deficiency 		22 0 14 8.0E-02 0 0
CUI: C0520927
Disease: Decreased fertility
Decreased fertility 		50 0 16 7.9E-02 0 0
CUI: C1384606
Disease: Dyspareunia
Dyspareunia 		37 0 15 7.9E-02 0 0
CUI: C4022003
Disease: Erectile abnormalities
Erectile abnormalities 		24 0 14 7.9E-02 0 0
CUI: C0003126
Disease: Anosmia
Anosmia 		40 0 15 7.8E-02 0 0
CUI: C1387005
Disease: Penis agenesis
Penis agenesis 		217 0 27 7.5E-02 0 0
CUI: C1827524
Disease: Wide spaced nipples
Wide spaced nipples 		96 0 18 7.3E-02 0 0
CUI: C1384583
Disease: Congenital absence of germinal epithelium of testes
Congenital absence of germinal epithelium of testes 		82 0 17 7.3E-02 0 0
CUI: C0454455
Disease: Mirror movements disorder
Mirror movements disorder 		39 0 14 7.3E-02 0 0
CUI: C0041408
Disease: Turner Syndrome
Turner Syndrome 		162 0 22 7.1E-02 0 0
CUI: C3489396
Disease: Hypogonadism, Isolated Hypogonadotropic
Hypogonadism, Isolated Hypogonadotropic 		42 0 14 7.1E-02 0 0
CUI: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly 		120 0 19 7.1E-02 0 0
CUI: C2364082
Disease: Sense of smell impaired
Sense of smell impaired 		60 0 15 7.0E-02 0 0
CUI: C2674432
Disease: Reduced bone mineral density
Reduced bone mineral density 		76 0 16 7.0E-02 0 0
CUI: C0685409
Disease: Congenital Camptodactyly
Congenital Camptodactyly 		123 0 19 7.0E-02 0 0
CUI: C4025821
Disease: Anterior hypopituitarism
Anterior hypopituitarism 		48 0 14 6.9E-02 0 0
CUI: C0220748
Disease: Cartilage-hair hypoplasia
Cartilage-hair hypoplasia 		49 0 14 6.9E-02 0 0
CUI: C0262444
Disease: Abnormality of the dentition
Abnormality of the dentition 		140 0 19 6.6E-02 0 0
CUI: C0030486
Disease: Paraplegia
Paraplegia 		59 0 14 6.6E-02 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect 		94 0 16 6.5E-02 0 0