Search Ontology:
Human Disease
Meier-Gorlin syndrome 2
- Term ID
- DOID:0080513
- Synonyms
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- Definition
- A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC4 gene on chromosome 2q23. https://www.omim.org/entry/613800
- References
- Ontology
- Human Disease ( DOID:0080513 )
- is a type of
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