Mild hypophosphatasia
MONDO:0600011The most common form of hypophosphatasia characterized by low alkaline phosphatase, unspecific clinical signs, and typically presents in individuals in adulthood. It is autosomal dominantly inherited.
Also known as: attenuated hypophosphatasia, HPPA, hypophosphatasia, adult
0 clinical trials for this condition and its sub-types.
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Disease
(680)
Metabolic disease
(233)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Human disease
(14)
Hypophosphatasia
(13)
Developmental defect during embryogenesis
(8)
Disease of genetic or genomic mechanism
(2)
ALPL-related autosomal dominant hypophosphatasia
(0)
Autosomal dominant disease
(0)
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