ALPL-related autosomal recessive hypophosphatasia
MONDO:0100609Any 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, 0 tagged with ALPL-related autosomal recessive hypophosphatasia itself.
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Browse by category →Sub-types of ALPL-related autosomal recessive hypophosphatasia
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Perinatal lethal hypophosphatasia 0 trials
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Severe hypophosphatasia 0 trials
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