Orofaciodigital syndrome XXI - CISMeF

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CISMeF

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Orofaciodigital syndrome XXIOMIM Phenotype

Preferred Label : Orofaciodigital syndrome XXI;

Symbol : OFD21;

Type : Phenotype, molecular basis known;

Prefixed ID : #301132;

Details

Origin ID

301132;

Genes related to phenotype
- Zinc finger-, ccch domain-, and rna-binding motif-containing serine/arginine-rich protein 2 [OMIM gene]

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21/08/2025

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