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

Full Report

Format

Full Report
Summary (Text)
Summary (XML)

Send to:

Choose Destination

File
Clipboard
Collections

Links from OMIM

Deafness, autosomal dominant nonsyndromic sensorineural 39, with dentinogenesis imperfecta 1

MedGen UID:: 864451
•Concept ID:: C4016014
•: Congenital Abnormality

Synonym:	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 39, WITH DENTINOGENESIS IMPERFECTA 1

OMIM®:	125485

Supplemental Content

Filter your results:

All (2)
Records in GTR (1)
Records in OMIM (2)
Diseases (2)
Records in Orphanet (0)
Records in HPO (0)
Records in Mondo (0)
Recommended for clinicians (1)

Manage Filters

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

Deafness, autosomal dominant nonsyndromic sensorineural 39, with dentinogenesis ...
Deafness, autosomal dominant nonsyndromic sensorineural 39, with dentinogenesis imperfecta 1

MedGen
MedGen for OMIM (Select 125485) (2)
MedGen

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...