Disease #01097 (MDDGA4;MEB;WWS (dystrophy-dystroglycanopathy, muscular, (congenital with brain and eye anomalies), type A4 (WWS, MEB)), OMIM:253800)

Official abbreviation MDDGA4;MEB;WWS
Name dystrophy-dystroglycanopathy, muscular, (congenital with brain and eye anomalies), type A4 (WWS, MEB)
OMIM ID 253800
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene FKTN
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2024-01-12 21:44:55 +01:00 (CET)

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