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
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.