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DO Term : childhood hypophosphatasia [DOID:0110915] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hypophosphatasia that has_material_basis_in an autosomal recessive mutation of the ALPL gene on chromosome 1p36.12.

synonyms:
ORDO:247667,
GARD:8735,
241510,
OMIM:241510

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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