Disease & disorder

infantile osteopetrosis with neuroaxonal dysplasia

MONDO:0010866

This syndrome is characterized by osteopetrosis, agenesis of the corpus callosum, cerebral atrophy and a small hippocampus.

Outbreak surveillance

Global reported events

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Clinical trials0
Recruiting0
Drug concepts studied0
Synonyms0
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Background context

infantile osteopetrosis with neuroaxonal dysplasia

Wikidata Q55999598 ↗
Background only. Canonical identity remains MONDO; clinical-trial relationships come from ClinicalTrials.gov.

Drugs being studied

Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.