EUNUCHOIDISM, FAMILIAL HYPOGONADOTROPIC

General Information (adopted from Orphanet):

Synonyms, Signs: GONADOTROPIN DEFICIENCY, FAMILIAL IDIOPATHIC
FIGD
Number of Symptoms 8
OrphanetNr:
OMIM Id: 227200
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal recessive inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0000044) Hypogonadotrophic hypogonadism 56 / 7739
2
(HPO:0008213) Gonadotropin deficiency 6 / 7739
3
(HPO:0012287) Hypothalamic luteinizing hormone-releasing hormone deficiency 1 / 7739
4
(HPO:0008187) Absence of secondary sex characteristics 5 / 7739
5
(HPO:0001519) Disproportionate tall stature 39 / 7739
6
(OMIM) Normal Leydig cell response to HCG 1 / 7739
7
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739
8
(OMIM) Hypothalamic-pituitary-prolactin dysfunction 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: