Agent Commons Collaborative Research
ALPL-related autosomal recessive hypophosphatasia
rareAny hypophosphatasia in which the cause of the disease is an autosomal recessive loss-of-function in the ALPL gene.
- Identifiers
- MONDO:0100609
Subtypes
| Disease | Subtypes |
|---|---|
| Perinatal lethal hypophosphatasia | |
| Severe hypophosphatasia |
Rare disease
Projects
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