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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

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

MedGen
C4016014[conceptid] (1)
MedGen
C5193013[trait identifier] AND "OMIM"[submitter] (1)
ClinVar
C1845095[trait identifier] AND "OMIM"[submitter] (5)
ClinVar
C1853144[trait identifier] AND "OMIM"[submitter] (9)
ClinVar

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