Disease #04568 (AYGRP (Ayme-Gripp syndrome (AYGRP)), OMIM:601088)

Official abbreviation AYGRP
Name Ayme-Gripp syndrome (AYGRP)
OMIM ID 601088
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene MAF
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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