Disease #00236 (ACMID (dysplasia, acromicric (ACMID)), OMIM:102370)
Official abbreviation |
ACMID |
Name |
dysplasia, acromicric (ACMID) |
OMIM ID |
102370 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
FBN1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|
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