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ALPL-related autosomal recessive hypophosphatasia

MONDO:0100609

Any hypophosphatasia in which the cause of the disease is an autosomal recessive loss-of-function in the ALPL gene.

0 clinical trials for this condition and its sub-types.

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Sub-types

Perinatal lethal hypophosphatasia (0) Severe hypophosphatasia (0)

Broader categories

Disease (680) Metabolic disease (233) Hereditary disease (176) Inborn errors of metabolism (45) Human disease (14) Hypophosphatasia (13) Developmental defect during embryogenesis (8) Autosomal recessive disease (4) Disease of genetic or genomic mechanism (2) Autosomal genetic disease (0)

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