OBO ID: DOID:0060291
Term Name: oculodentodigital dysplasia Search Ontology:
Synonyms:
  • ODD syndrome
Definition: A syndrome characterized by craniofacial, neurologic, limb and ocular abnormalities. (3)
References:
Ontology: Human Disease   (DOID:0060291)
Relationships
is a type of:
OTHER oculodentodigital dysplasia PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GJA1 Oculodentodigital dysplasia 164200
Oculodentodigital dysplasia, autosomal recessive 257850
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None