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Grange syndrome

Synonyms
GRANGE OCCLUSIVE ARTERIAL SYNDROME
Modes of inheritance
Autosomal recessive inheritance (Orphanet)
Autosomal dominant inheritance (Orphanet)

Summary

Grange syndrome (GRNG) is a rare early-onset disease characterized by hypertension and multifocal stenoocclusive lesions of renal, cerebral, and abdominal arteries. Bone fragility, syndactyly, brachydactyly, congenital heart defects, and learning disabilities have been reported with variable expressivity and incomplete penetrance (summary by Rath et al., 2019). [from OMIM]

Available tests

6 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (6 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: GRNG, HCCA1, HCCA2, YY1AP, YY1AP1
    Summary: YY1 associated protein 1

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

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