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Disease Ontology Browser
otopalatodigital syndrome type 2 (DOID:0111784)
Alliance: disease page
Synonyms: Andre syndrome; faciopalatoosseous syndrome; OPD2; OPD II syndrome; OPD syndrome 2; oto-palato-digital syndrome type 2; otopalatodigital syndrome type II
Alt IDs: OMIM:304120, MESH:C538089, ORDO:90652, UMLS_CUI:C1844696
Definition: An otopalatodigital syndrome spectrum disorder characterized by disabling skeletal anomalies and variable malformations in the hindbrain, heart, intestines, and kidneys that frequently lead to perinatal death in males and less severe phenotypes in females that has_material_basis_in hemizygous or heterozygous mutation in exons 3, 4, or 5 in males or exons 28 or 29 in females of the FLNA gene on chromosome Xq28.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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11/12/2024
MGI 6.24 		The Jackson Laboratory