MEND syndrome

Summary
Synonym
  • male EBP disorder with neurological defects
Definition
A lipid metabolism disorder characterized by a defect in sterol biosynthesis that results in variable features including intellectual disability, short stature, scoliosis, digital abnormalities, cataracts, and dermatologic abnormalities that has_material_basis_in hemizygous mutation in EBP on chromosome Xp11.23.
Super Class
X-linked recessive disease lipid metabolism disorder
External Links
Disease Ontology
DOID:0111865
Mondo Disease Ontology
UMLS
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
10682 EBP EBP cholestenol delta-isomerase
The Human Phenotype Ontology
Displaying entries 61 - 63 of 63 in total
HPO ID HPO Term
HP:0007663 Reduced visual acuity
HP:0008936 Axial hypotonia
HP:0010442 Polydactyly
Displaying 1 entry
Gene ID Gene Symbol Description
10682 EBP EBP cholestenol delta-isomerase

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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