Search Ontology:
Human Disease

childhood hypophosphatasia

Term ID
DOID:0110915
Synonyms
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
References
Ontology
Human Disease   ( DOID:0110915 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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