Table B. [OMIM Entries for Hypohidrotic Ectodermal Dysplasia (View All in OMIM)]. - GeneReviews® - NCBI Bookshelf

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Table B.

OMIM Entries for Hypohidrotic Ectodermal Dysplasia (View All in OMIM)

129490	ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT; ECTD10A
224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B
300451	ECTODYSPLASIN A; EDA
305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED
604095	ECTODYSPLASIN A RECEPTOR; EDAR
606268	WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 10A; WNT10A
606603	EDAR-ASSOCIATED DEATH DOMAIN; EDARADD
614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B

From: Hypohidrotic Ectodermal Dysplasia

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Wright JT, Grange DK, Fete M. Hypohidrotic Ectodermal Dysplasia. 2003 Apr 28 [Updated 2022 Oct 27]. In: Adam MP, Feldman J, Mirzaa GM, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2024. Table B. [OMIM Entries for Hypohidrotic Ectodermal Dysplasia (View All in OMIM)].
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