Disease #01877 (HH3 (hypogonadotropic hypogonadism, type 3 with/without anosmia (HH-3)), OMIM:244200)
Official abbreviation |
HH3 |
Name |
hypogonadotropic hypogonadism, type 3 with/without anosmia (HH-3) |
OMIM ID |
244200 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
PROKR2 |
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) |
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