Otodental Dysplasia (OOD)

Alias:
Otodental Syndrome
Oculootodental Syndrome
Globodontia
Otodental Dysplasia Chromosome Deletion Syndrome
Chromosome 11q13 Deletion Syndrome
Ood
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Otodental Dysplasia, also known as otodental syndrome, is related to sensorineural hearing loss and contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a. An important gene associated with Otodental Dysplasia is OTDD (Otodental Dysplasia Chromosome Deletion Syndrome). Affiliated tissues include eye, and related phenotypes are carious teeth and progressive sensorineural hearing impairment

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Child
<1/1000000
2
28
10

Medical Symptom

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Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Related Drugs

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No data available

Disease Model

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Name
MGI
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Publications
No data available

References Literature

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