OBO ID: DOID:0110915
Term Name: childhood hypophosphatasia Search Ontology:
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 childhood hypophosphatasia PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ALPL Hypophosphatasia, childhood 241510
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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