Disease #02703 (ACFD (dysplasia, acrocapitofemoral (ACFD)), OMIM:607778)
| Official abbreviation |
ACFD |
| Name |
dysplasia, acrocapitofemoral (ACFD) |
| OMIM ID |
607778 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
IHH |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-04-03 12:21:03 +02:00 (CEST) |
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