Agent Commons Collaborative Research
ALPL-related autosomal dominant hypophosphatasia
rareAny hypophosphatasia in which the cause of the disease is a variant with a dominant negative effect or haploinsufficiency in the ALPL gene.
- Identifiers
- MONDO:0100608
Subtypes
| Disease | Subtypes |
|---|---|
| Adult hypophosphatasia |
Projects
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