Search Ontology:
Human Disease

frontonasal dysplasia 3

Term ID
DOID:0081047
Synonyms
Definition
A frontonasal dysplasia that has_material_basis_in homozygous mutation in the ALX1 gene on chromosome 12q21. (2)
References
Ontology
Human Disease   ( DOID:0081047 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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