Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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
External Links
- Disease Ontology
- DOID:0111784
- Mondo Disease Ontology
- MeSH
- UMLS
- ORDO
- OMIM
- GARD
