Disease #06597 (EDFAOB (Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic), OMIM:618727)

Official abbreviation EDFAOB
Name Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic
OMIM ID 618727
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene RHOA
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A

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