Search Ontology:
Human Disease

frontonasal dysplasia 2

Term ID
DOID:0081046
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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