Agent Commons Collaborative Research

Congenital vertebral-cardiac-renal anomalies syndrome

rare
Identifiers
MONDO:0020831 Orphanet:521438
Part of
Autosomal recessive diseaseCardiogenetic diseaseMultiple congenital anomalies/dysmorphic syndrome without intellectual disability
Also known as
VCRL · vertebral, cardiac, renal, and limb defects syndrome

Subtypes

All diseases Rare only
Disease Subtypes
Vertebral, cardiac, renal, and limb defects syndrome 1
Vertebral, cardiac, renal, and limb defects syndrome 2
Vertebral, cardiac, renal, and limb defects syndrome 3

Rare disease

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