ALPL-related autosomal dominant hypophosphatasia

MONDO:0100608

Any hypophosphatasia in which the cause of the disease is a variant with a dominant negative effect or haploinsufficiency in the ALPL gene.

0 clinical trials for this condition and its sub-types, 0 tagged with ALPL-related autosomal dominant hypophosphatasia itself.

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Sub-types of ALPL-related autosomal dominant hypophosphatasia

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