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
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
Displaying 1 entry
Gene ID Gene Symbol Description Source
13595 Ebp EBP cholestenol delta-isomerase
The Human Phenotype Ontology
Displaying entries 1 - 10 of 63 in total
HPO ID HPO Term
HP:0000028 Cryptorchidism
HP:0000175 Cleft palate
HP:0000218 High palate
HP:0000238 Hydrocephalus
HP:0000260 Wide anterior fontanel
HP:0000316 Hypertelorism
HP:0000347 Micrognathia
HP:0000369 Low-set ears
HP:0000422 Abnormal nasal bridge morphology
HP:0000426 Prominent nasal bridge
Displaying 1 entry
Gene ID Gene Symbol Description
10682 EBP EBP cholestenol delta-isomerase

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Last updated: December 9, 2024