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Metadata
ID	DOID:0081290
Name	Antley-Bixler syndrome without disordered steroidogenesis
Definition	An Antley-Bixler syndrome that has_material_basis_in heterozygous mutation in a fibroblast growth factor receptor gene, FGFR2, on chromosome 10q26 and is an exclusively skeletal form of Antley-Bixler syndrome. https://pubmed.ncbi.nlm.nih.gov/15793702/
Xrefs	MIM:207410
Parent Relationships	is_a autosomal dominant disease is_a Antley-Bixler syndrome
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance