otopalatodigital syndrome type 2

Term ID

DOID:0111784

Synonyms

• Andre syndrome
• faciopalatoosseous syndrome
• OPD II syndrome
• OPD syndrome 2
• OPD2
• oto-palato-digital syndrome type 2
• otopalatodigital syndrome type II

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. (3)

References

• GARD:5802
• MESH:C538089
• OMIM:304120
• ORDO:90652
• SNOMEDCT_US_2023_03_01:42432003
• UMLS_CUI:C1844696

Ontology

Human Disease   ( DOID:0111784 )