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MedGen

National Center for Biotechnology Information

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Items: 3

Select item 4101431.

Tooth agenesis, selective, X-linked, 1

Any tooth agenesis in which the cause of the disease is a mutation in the EDA gene. [from MONDO]

MedGen UID:: 410143
•Concept ID:: C1970757
•: Disease or Syndrome

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 3189372.

Otodental syndrome

Otodental syndrome is an autosomal dominant condition characterized by grossly enlarged canine and molar teeth (globodontia), associated with sensorineural hearing loss. Ocular coloboma segregating with otodental syndrome has been reported (summary by Gregory-Evans et al., 2007). [from OMIM]