Disease #00090 (ECTD9 (dysplasia, ectodermal, type 9, hair/nail (ECTD-9)), OMIM:614931)
| Official abbreviation |
ECTD9 |
| Name |
dysplasia, ectodermal, type 9, hair/nail (ECTD-9) |
| OMIM ID |
614931 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
HOXC13 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2012-12-05 08:26:23 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|