oculodentodigital

oc·u·lo·den·to·dig·i·tal

(ok'yū-lō-den'tō-dij'i-tăl),
Relating to the eyes, teeth, and fingers.

oc·u·lo·den·to·dig·i·tal

(ok'yū-lō-den'tō-dij'i-tăl)
Relating to eyes, teeth, and fingers.
References in periodicals archive ?
Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia.
But it should be kept in mind that microphthalmia, which is one of the most common feature in many syndromes can also be observed in Micro syndrome (4), oculodentodigital dysplasia (5,6) (ODDD), oculofaciocardiodental syndrome (7) (OFCDS), and Lenz microphthalmia syndrome (1-3).
Oculodentodigital dysplasia (ODDD) is a rare autosomal dominant inherited disorder affecting the development of the face, eyes, teeth, and limbs.

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