Disease #00595 (HCH (hypochondroplasia (HCH)), OMIM:146000)
Official abbreviation |
HCH |
Name |
hypochondroplasia (HCH) |
OMIM ID |
146000 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
FGFR3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-10-22 16:16:54 +02:00 (CEST) |
Individuals
|