Disease #02019 (CPHD4 (hormone deficiency, pituitary, combined, type 4), OMIM:262700)
Official abbreviation |
CPHD4 |
Name |
hormone deficiency, pituitary, combined, type 4 |
OMIM ID |
262700 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
7 |
Phenotype entries for this disease |
6 |
Associated with 1 gene |
LHX4 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2022-12-24 13:48:38 +01:00 (CET) |
Individuals
|