Search Ontology:
Human Disease
Meier-Gorlin syndrome 6
- Term ID
- DOID:0080517
- Synonyms
-
- Definition
- A Meier-Gorlin syndrome that has_material_basis_in heterozygous mutation in the GMNN gene on chromosome 6p22. https://www.omim.org/entry/616835
- References
- Ontology
- Human Disease ( DOID:0080517 )
- is a type of
-
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