Disease #01748 (CPHD3 (hormone deficiency, pituitary, combined, type 3), OMIM:221750)
| Official abbreviation |
CPHD3 |
| Name |
hormone deficiency, pituitary, combined, type 3 |
| OMIM ID |
221750 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
LHX3 |
| Associated tissues |
- |
| Disease features |
autosomal recessive |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2022-12-22 16:34:37 +01:00 (CET) |
Individuals
|