Disease & disorder

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12

MONDO:0014101

Any muscular dystrophy-dystroglycanopathy, type A in which the cause of the disease is a mutation in the POMK gene.

Outbreak surveillance

Global reported events

Explore recent public health notices potentially related to muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12. Results are keyword matches, not yet verified disease-to-outbreak relationships.

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Clinical trials0
Recruiting0
Drug concepts studied0
Synonyms4
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Background context

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12

Wikidata Q66084931 ↗
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.