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 0
Phenotype entries for this disease 0
Associated with 1 gene MAF
Associated tissues -
Disease features -
Remarks -

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