microphthalmia with limb anomalies

Summary
Synonym
  • MLA
  • OAS
  • Waardenburg anophthalmia syndrome
  • anophthalmia-syndactyly syndrome
  • ophthalmoacromelic syndrome
Definition
A syndrome that is characterized by autosomal recessive inheritance of bilateral or unilateral clinical anophthalmia or microphthalmia and synostosis, syndactyly, oligodactyly and/or polydactyly that has_material_basis_in homozygous mutation in the SMOC1 gene on chromosome 14q24.
Super Class
autosomal recessive disease syndrome
External Links
Disease Ontology
DOID:0060861
Mondo Disease Ontology
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying all 4 entries
Gene ID Gene Symbol Description Source
4968 OGG1 8-oxoguanine DNA glycosylase
5290 PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha
8809 IL18R1 interleukin 18 receptor 1
55556 ENOSF1 enolase superfamily member 1
Related Glycoprotein

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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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