Disease #00084 (ACMICD (ACROMICRIC DYSPLASIA), OMIM:102370)

MVZ für Humangenetik Regensburg

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Official abbreviation	ACMICD
Name	ACROMICRIC DYSPLASIA
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	2023-06-16 09:12:48 +00:00 (UTC)
Date last edited	N/A