Search Ontology:
Human Disease
Meier-Gorlin syndrome 7
- Term ID
- DOID:0080518
- Synonyms
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- Definition
- A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CDC45 gene on chromosome 22q11. https://pubmed.ncbi.nlm.nih.gov/27374770/
- References
- Ontology
- Human Disease ( DOID:0080518 )
- is a type of
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