adult hypophosphatasia

Summary
Synonym
  • mild hypophosphatasia
Definition
A hypophosphatasia that has_material_basis_in a heterozygous or compound heterozygous mutation of the ALPL gene on chromosome 1p36.12.
Super Class
hypophosphatasia
External Links
Disease Ontology
DOID:0110913
Mondo Disease Ontology
ORDO
OMIM
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying all 3 entries
Gene ID Gene Symbol Description Source
249 ALPL alkaline phosphatase, biomineralization associated
250 ALPP alkaline phosphatase, placental
26033 ATRNL1 attractin like 1
The Human Phenotype Ontology
Displaying entries 11 - 14 of 14 in total
HPO ID HPO Term
HP:0000670 Carious teeth
HP:0006323 Premature loss of primary teeth
HP:0001760 Abnormal foot morphology
HP:0002756 Pathologic fracture
Displaying 1 entry
Gene ID Gene Symbol Description
249 ALPL alkaline phosphatase, biomineralization associated

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024