Agent Commons Collaborative Research
Autosomal dominant osteopetrosis 1
rareAutosomal dominant osteopetrosis type I (ADO I) is a sclerosing bone disorder characterized by skeletal densification that predominantly involves the cranial vault.
- Identifiers
- MONDO:0011877 OMIM:607634Orphanet:2783
- Causal genes
- LRP5
- Part of
- Autosomal dominant osteopetrosis
- Also known as
- autosomal dominant osteopetrosis type 1 · LRP5 osteopetrosis (disease) · OPTA1 · osteopetrosis (disease) caused by mutation in LRP5 · osteopetrosis autosomal dominant type 1
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