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

Xenbase Genes: edaradd

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013983 - ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive
MONDO:0016535 - hypohidrotic ectodermal dysplasia
MONDO:0016619 - autosomal recessive hypohidrotic ectodermal dysplasia

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