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Microtia
2 OMIM references -
1 associated gene
5 connected diseases
No signs/symptoms info
Disease Type of connection
Anotia
Bilateral microtia - deafness - cleft palate
Hydranencephaly
Microlissencephaly
Steinert myotonic dystrophy
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare otorhinolaryngologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
1 MeSH reference: C537772
Gene symbol UniProt reference OMIM reference
HOXA2 O43364604685
No signs/symptoms info available.