alopecia-mental retardation syndrome 4

Summary
Definition
An alopecia-mental retardation syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the LSS gene on chromosome 21q22.
Super Class
alopecia-mental retardation syndrome autosomal recessive disease
External Links
Disease Ontology
DOID:0080950
Mondo Disease Ontology
OMIM
WikiPathways (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
4047 LSS lanosterol synthase
The Human Phenotype Ontology
Displaying entries 1 - 10 of 35 in total
HPO ID HPO Term
HP:0002353 EEG abnormality
HP:0001249 Intellectual disability
HP:0200012 Short corpus callosum
HP:0000613 Photophobia
HP:0005105 Abnormal nasal morphology
HP:0001510 Growth delay
HP:0000365 Hearing impairment
HP:0002750 Delayed skeletal maturation
HP:0001252 Hypotonia
HP:0011842 Abnormal skeletal morphology
Displaying 1 entry
Gene ID Gene Symbol Description
4047 LSS lanosterol synthase

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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