otopalatodigital syndrome type 2

Summary
Synonym
  • Andre syndrome
  • OPD II syndrome
  • OPD syndrome 2
  • OPD2
  • faciopalatoosseous syndrome
  • 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.
Super Class
X-linked dominant disease otopalatodigital syndrome spectrum disorder
Disease Ontology
DOID:0111784
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
2316 FLNA filamin A

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024