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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