Disease #00951 (Scaphocephaly and Axenfeld-Rieger anomaly)

Official abbreviation -
Name Scaphocephaly and Axenfeld-Rieger anomaly
OMIM ID -
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene FGFR2
Associated tissues -
Disease features -
Remarks -

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