Warning: The NCBI web site requires JavaScript to function. more...

MedGen

National Center for Biotechnology Information

Full Report

Format

Full Report
Summary (Text)
Summary (XML)

Send to:

Choose Destination

File
Clipboard
Collections

Ectodermal dysplasia 10a, hypohidrotic/hair/tooth type, autosomal dominant

MedGen UID:: 764501
•Concept ID:: C3551587
•: Finding

Synonym:	ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT

OMIM®:	604095

Supplemental Content

Table of contents

Clinical resources

ClinicalTrials.gov

Consumer resources

MedlinePlus

Reviews

Related information

ClinVar
Related medical variations
OMIM
Related records in OMIM
PubMed (OMIM)
Related literature resources in PubMed

Recent activity

Clear Turn Off Turn On

Ectodermal dysplasia 10a, hypohidrotic/hair/tooth type, autosomal dominant
Ectodermal dysplasia 10a, hypohidrotic/hair/tooth type, autosomal dominant

MedGen
C3551587[conceptid] (1)
MedGen
C3887494[trait identifier] AND "OMIM"[submitter] (10)
ClinVar
C3809665[trait identifier] AND "OMIM"[submitter] (4)
ClinVar
C5567229[trait identifier] AND "OMIM"[submitter] (3)
ClinVar

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...