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: C1563720
Disease: Kallmann Syndrome 2 (disorder)
Kallmann Syndrome 2 (disorder) 		8 0 6 0.75 0 0
CUI: C1720275
Disease: Gonadotropin releasing factor deficiency
Gonadotropin releasing factor deficiency 		5 0 4 0.57 0 0
CUI: C1563719
Disease: Kallmann Syndrome 1
Kallmann Syndrome 1 		12 0 6 0.50 0 0
CUI: C4022675
Disease: Increased female libido
Increased female libido 		18 0 6 0.33 0 0
CUI: C4025901
Disease: Abnormality of body height
Abnormality of body height 		18 0 6 0.33 0 0
CUI: C4025569
Disease: Eunuchoid habitus
Eunuchoid habitus 		21 0 6 0.29 0 0
CUI: C4025644
Disease: Hypothalamic gonadotropin-releasing hormone deficiency
Hypothalamic gonadotropin-releasing hormone deficiency 		22 0 6 0.27 0 0
CUI: C1846228
Disease: Absence of pubertal development
Absence of pubertal development 		24 0 6 0.25 0 0
CUI: C4022003
Disease: Erectile abnormalities
Erectile abnormalities 		24 0 6 0.25 0 0
CUI: C0271578
Disease: Female hypogonadism syndrome
Female hypogonadism syndrome 		25 0 6 0.24 0 0
CUI: C0234362
Disease: Synkinesis
Synkinesis 		13 0 3 0.19 0 0
CUI: C0338503
Disease: Septo-Optic Dysplasia
Septo-Optic Dysplasia 		35 0 6 0.17 0 0
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		8 0 2 0.17 0 0
CUI: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type 		1 0 1 0.17 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome 		1 0 1 0.17 0 0
CUI: C0266384
Disease: Congenital absence of uterus
Congenital absence of uterus 		1 0 1 0.17 0 0
CUI: C0266692
Disease: Craniopagus
Craniopagus 		1 0 1 0.17 0 0
CUI: C0432149
Disease: Lumbar hemivertebra
Lumbar hemivertebra 		1 0 1 0.17 0 0
CUI: C0795829
Disease: Chromosome 8, trisomy 8q
Chromosome 8, trisomy 8q 		1 0 1 0.17 0 0
CUI: C1168263
Disease: Central Hypogonadism
Central Hypogonadism 		1 0 1 0.17 0 0
CUI: C1333286
Disease: Diencephalic Neoplasm
Diencephalic Neoplasm 		1 0 1 0.17 0 0
CUI: C1845146
Disease: Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate 		1 0 1 0.17 0 0
CUI: C3495417
Disease: Hemifacial microsomia
Hemifacial microsomia 		8 0 2 0.17 0 0
CUI: C3550478
Disease: HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA
HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA 		1 0 1 0.17 0 0
CUI: C3552136
Disease: HYPOGONADOTROPHIC HYPOGONADISM 5 WITHOUT ANOSMIA
HYPOGONADOTROPHIC HYPOGONADISM 5 WITHOUT ANOSMIA 		1 0 1 0.17 0 0