Disease #00672 (ABS2 (Antley-Bixler syndrome, without genital anomalies or disordered steroidogenesis (ABS-2)), OMIM:207410)

Official abbreviation ABS2
Name Antley-Bixler syndrome, without genital anomalies or disordered steroidogenesis (ABS-2)
OMIM ID 207410
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene FGFR2
Associated tissues -
Disease features -
Remarks -