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 -
Phenotype entries for this disease -
Associated with 1 gene FBN1
Associated tissues -
Disease features -
Remarks -
Date created 2013-10-09 21:31:37 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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