Search Ontology:
Human Disease
Meier-Gorlin syndrome 1
- Term ID
- DOID:0080512
- Synonyms
-
- Definition
- A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC1 gene on chromosome 1p32. https://www.omim.org/entry/224690
- References
- Ontology
- Human Disease ( DOID:0080512 )
- is a type of
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