Small eyes, enamel defects and syndactyly.
- Specialty
- Dentistry
- Subspecialty
- Dentistry / Pediatric dentistry
- Sex & age distribution
- Male: affected; Female: affected; Children: yes
- Gene(s) involved
- GJA1
- Alternative names & eponyms
- ODDD
Etiology & mechanism
GJA1 mutation.
Gene(s) involved (1)
Symptoms & signs (4)
In plain terms, someone with Oculodentodigital dysplasia syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
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Shares symptoms with
1 shared
Amelogenesis imperfecta with nephrocalcinosis syndrome
enamel hypoplasia
1 shared
Apert syndrome
syndactyly
1 shared
Autoimmune polyglandular syndrome type 1
enamel hypoplasia
1 shared
Cross syndrome
microphthalmia
1 shared
Fraser syndrome
syndactyly
1 shared
Hallermann–Streiff syndrome
microphthalmia
1 shared
Orofaciodigital syndrome type 1
syndactyly
1 shared
Patau syndrome
microphthalmia
1 shared
Potocki–Shaffer syndrome
syndactyly
1 shared
Timothy syndrome
syndactyly
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