OBO ID: DOID:0110915 |
Term Name: | childhood hypophosphatasia | Search Ontology: | |
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Definition: | A hypophosphatasia that has_material_basis_in an autosomal recessive mutation of the ALPL gene on chromosome 1p36.12. https://www.ncbi.nlm.nih.gov/pubmed/1409720 | ||
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Ontology: | Human Disease ( DOID:0110915 ) |
OTHER childhood hypophosphatasia PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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