Disease #01388 (HH7 (hypogonadism, hypogonadotropic, type 7 (HH7)), OMIM:146110)
Official abbreviation |
HH7 |
Name |
hypogonadism, hypogonadotropic, type 7 (HH7) |
OMIM ID |
146110 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
4 |
Phenotype entries for this disease |
4 |
Associated with 5 genes |
FGFR1, FSHB, GNRH1, GNRHR, WDR11 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|