Infantile hypophosphatasia
MONDO:1010169Infantile hypophosphatasia (I-HPP) is a very rare, severe form of hypophosphatasia characterized by infantile rickets without elevated serum alkaline phosphatase (ALP) activity and a wide range of clinical manifestations due to hypomineralization.
Also known as: infantile hypophosphatasia
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
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Inborn errors of metabolism
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Human disease
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Hypophosphatasia
(13)
Developmental defect during embryogenesis
(8)
Disease of genetic or genomic mechanism
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Developmental anomaly of metabolic origin
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Disease by developmental or physiological process
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