OBO ID: DOID:0081046
Term Name: frontonasal dysplasia 2 Search Ontology:
Synonyms:
Definition: A frontonasal dysplasia that has_material_basis_in homozygous mutation in the ALX4 gene on chromosome 11p11. https://pubmed.ncbi.nlm.nih.gov/22140057/
References:
Ontology: Human Disease   ( DOID:0081046 )
Relationships
is a type of:
OTHER frontonasal dysplasia 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ALX4 Frontonasal dysplasia 2 613451
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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