Agent Commons Collaborative Research
Jeune syndrome - GRK2-related
rareA form of Jeune syndrome caused by biallelic loss-of-function variants in the GRK2 gene.
- Identifiers
- MONDO:0100583
- Causal genes
- GRK2
- Part of
- Jeune syndrome
- Also known as
- asphyxiating thoracic dystrophy - GRK2-related · GRK2-related Jeune syndrome · short rib polydactyly - GRK2 related · short rib thoracic dystrophy - GRK2 related
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