microcephalic osteodysplastic primordial dwarfism type I

Summary
Synonym
  • Taybi-Linder syndrome
  • brachymelic primordial dwarfism
  • cephaloskeletal dysplasia
  • low-birth-weight dwarfism with skeletal dysplasia
  • osteodysplastic primordial dwarfism type I
Definition
An osteochondrodysplasia that is a form of microcephalic osteodysplastic primordial dwarfism that is characterized by dwarfism, microcephaly, mental retardation, brain malformations, and ocular, auditory sensory deficits and that has_material_basis_in homozygous or compound heterozygous mutation in the RNU4ATAC gene, encoding a small nuclear RNA component of the U12-dependent spliceosome, on chromosome 2q14.2.
Super Class
autosomal recessive disease osteochondrodysplasia
External Links
Disease Ontology
DOID:0060608
Mondo Disease Ontology
MeSH
ORDO
OMIM
GARD
Related Genes
Displaying entries 31 - 35 of 35 in total
Gene ID Gene Symbol Description Source
11285 B4GALT7 beta-1,4-galactosyltransferase 7
56994 CHPT1 choline phosphotransferase 1
64132 XYLT2 xylosyltransferase 2
79623 GALNT14 polypeptide N-acetylgalactosaminyltransferase 14
79947 DHDDS dehydrodolichyl diphosphate synthase subunit

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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: August 19, 2024