osteopetrosis (Q17131): Difference between revisions
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Created claim: instance of (P2): rare disease (Q12388) |
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_667 |
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| Property / instance of: class of disease / rank | |||
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| Property / subclass of: osteosclerosis / rank | |||
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| Property / subclass of: disease / rank | |||
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| Property / health specialty: medical genetics / rank | |||
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| Property / exact match: http://purl.obolibrary.org/obo/DOID_13533 / rank | |||
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| Property / exact match: http://identifiers.org/doid/DOID:13533 / rank | |||
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| Property / exact match | |||
| Property / exact match: http://www.orpha.net/ORDO/Orphanet_667 / rank | |||
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Latest revision as of 21:01, 29 December 2023
an extremely rare inherited disorder whereby the bones harden, becoming denser, sometimes causing bones to dissolve and break, caused by malfunctioning osteoclasts’ inability to resorb bone
- Albers-Schonberg disease
- marble bone
- marble bone disease
- Albers-Schönberg disease
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | osteopetrosis |
an extremely rare inherited disorder whereby the bones harden, becoming denser, sometimes causing bones to dissolve and break, caused by malfunctioning osteoclasts’ inability to resorb bone |
|