Prenatal benign hypophosphatasia
MONDO:0700424A very rare form of hypophosphatasia characterized by prenatal skeletal manifestations (limb shortening and bowing) that slowly resolve spontaneously and later may develop into the moderate childhood or adult forms of the disease.
0 clinical trials for this condition and its sub-types.
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Disease
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Metabolic disease
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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)
Developmental anomaly of metabolic origin
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Disease by developmental or physiological process
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