Search Ontology:
Human Disease
Meier-Gorlin syndrome 4
- Term ID
- DOID:0080515
- Synonyms
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- Definition
- A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CDT1 gene on chromosome 16q24. https://www.omim.org/entry/613804
- References
- Ontology
- Human Disease ( DOID:0080515 )
- is a type of
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