Search Ontology:
Human Disease
orofaciodigital syndrome XIV
- Term ID
- DOID:0060958
- Synonyms
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- Definition
- An orofaciodigital syndrome that is characterized by severe microcephaly, trigonocephaly, severe intellectual disability and micropenis, in addition to oral, facial and digital malformations (gingival frenulae, lingual hamartomas, cleft/lobulated tongue, cleft palate, telecanthus, up-slanting palpebral fissures, microretrognathia, postaxial polydactyly of hands and duplication of hallux) that has_material_basis_in homozygous or compound heterozygous mutation in the C2CD3 gene on chromosome 11q13. https://pubmed.ncbi.nlm.nih.gov/24997988/
- References
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- GARD:13655
- MIM:615948
- ORDO:434179
- Ontology
- Human Disease ( DOID:0060958 )
- is a type of
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Genes Involved
Zebrafish Models