Kahrizi syndrome

Summary
Synonym
  • KHRZ
  • intellectual disability, Kahrizi type
  • intellectual disability-cataract-coloboma-kyphosis syndrome
Definition
A syndrome that is characterized by mental retardation, cataracts, coloboma, kyphosis, and coarse facial features and has_material_basis_in mutation in the SRD5A3 gene.
Super Class
autosomal recessive disease syndrome
External Links
Disease Ontology
DOID:0050807
Mondo Disease Ontology
MeSH
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
79644 SRD5A3 steroid 5 alpha-reductase 3
The Human Phenotype Ontology
Displaying entries 11 - 15 of 15 in total
HPO ID HPO Term
HP:0000518 Cataract
HP:0012471 Thick vermilion border
HP:0001250 Seizure
HP:0000414 Bulbous nose
HP:0003593 Infantile onset
Displaying 1 entry
Gene ID Gene Symbol Description
79644 SRD5A3 steroid 5 alpha-reductase 3

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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