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Summary Literature (0)
OMIM:614941 - ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B


In Disease Ontology (DO):
DOID:0111654 - ectodermal dysplasia 11B

In Mondo Disease Ontology:
MONDO:0013983 - ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive

Human Disease Resources: OMIM

Xenbase Genes: edaradd