multiple epiphyseal dysplasia 4

Summary
Synonym
  • EDM4
  • MED4
  • Polyepiphyseal dysplasia type 4
  • multiple epiphyseal dysplasia with bilateral patellae
  • multiple epiphyseal dysplasia with clubfoot
  • rMED
Definition
A multiple epiphyseal dysplasia that has_material_basis_in homozygous mutation in the SLC26A2 gene on chromosome 5q32.
Super Class
autosomal recessive disease multiple epiphyseal dysplasia
Disease Ontology
DOID:0070300
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
WikiPathways (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
1836 SLC26A2 solute carrier family 26 member 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
13521 Slc26a2 solute carrier family 26 (sulfate transporter), member 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
117267 Slc26a2 solute carrier family 26 member 2
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
P50443 Sulfate transporter
The Human Phenotype Ontology
Displaying entries 1 - 10 of 57 in total
HPO ID HPO Term
HP:0000175 Cleft palate
HP:0000218 High palate
HP:0000347 Micrognathia
HP:0000363 Abnormal earlobe morphology
HP:0000369 Low-set ears
HP:0000377 Abnormal pinna morphology
HP:0001156 Brachydactyly
HP:0001371 Flexion contracture
HP:0001376 Limitation of joint mobility
HP:0001385 Hip dysplasia
Displaying 1 entry
Gene ID Gene Symbol Description
1836 SLC26A2 solute carrier family 26 member 2

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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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