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[NTR/gene] ALPL-related autosomal recessive hypophosphatasia #8755
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Hi @RyanFWebb thanks for your ticket. Is this new term related to any of these terms?
(See related ticket: #2906) |
@sabrinatoro I'd like to discuss this on the curation call:
|
@nicolevasilevsky I've updated the disease term to be consistent with the term for autosomal dominant hypophosphatasia. Additionally, 'moderate hypophosphatasia', 'odontohypophosphatasia', 'perinatal lethal hypophosphatasia', and 'severe hypophosphatasia' would be listed as children. |
) * add gene info to hypophosphatasia address #8755 * add new terms: 'ALPL-related autosomal dominant hypophosphatasia' and 'ALPL-related autosomal recessive hypophosphatasia' * fix xref and add github
Preferred gene-related syndrome label
ALPL-related autosomal recessive hypophosphatasia
Synonyms
Parent term (use OLS, or your favorite ontology browser)
hypophosphatasia
Definition
Any autosomal recessive hypophosphatasia in which the cause of the disease is loss-of-function in the ALPL gene.
Definition source (Please give PubMed ID, if applicable, in format PMID:#######)
On behalf of ClinGen's Skeletal Disorders Gene Curation Expert Panel.
Children terms (if applicable) Should any existing terms be re-classified as children underneath this new proposed term?
'moderate hypophosphatasia'
'odontohypophosphatasia'
'perinatal lethal hypophosphatasia'
'severe hypophosphatasia'
Your nano-attribution (ORCID) or URL for a working group
ClinGen's Skeletal Disorders Gene Curation Expert Panel
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