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Summary Literature (0)
DOID:0110915 - childhood hypophosphatasia

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

Synonyms:

Xenbase Genes : alpl

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009428 - obsolete childhood hypophosphatasia

MIM:
MIM:241510 - HYPOPHOSPHATASIA, CHILDHOOD; HPPC

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hypophosphatasia (is_a)