ALPL-related autosomal dominant hypophosphatasia mild hypophosphatasia https://github.com/monarch-initiative/mondo/issues/8755 https://github.com/monarch-initiative/mondo/issues/9867 The 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. GARD:0026295 HPPA This term is scheduled to be merged with MONDO:1010154 adult hypophosphatasia, based on the fact that the concept of these 2 terms are the same. This ID will therefore be obsoleted and replaced with MONDO:1010154 attenuated hypophosphatasia 2026-04-01 MONDO:0600011