hypotrichosis 12

Summary
Synonym
  • Hypt12
Definition
A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the RPL21 gene on chromosome 13q12.2.
Super Class
autosomal dominant disease hypotrichosis
Disease Ontology
DOID:0110709
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6144 RPL21 ribosomal protein L21
The Human Phenotype Ontology
Displaying all 5 entries
HPO ID HPO Term
HP:0001596 Alopecia
HP:0002231 Sparse body hair
HP:0000653 Sparse eyelashes
HP:0008070 Sparse hair
HP:0002209 Sparse scalp hair
Displaying all 2 entries
Gene ID Gene Symbol Description
4047 LSS lanosterol synthase
200879 LIPH lipase H

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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: December 9, 2024