VCRL3
MCID: VRT017
MIFTS: 16
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Vertebral, Cardiac, Renal, and Limb Defects Syndrome 3 (VCRL3)
Categories:
Genetic diseases, Nephrological diseases
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MalaCards integrated aliases for Vertebral, Cardiac, Renal, and Limb Defects Syndrome 3:
Name: Vertebral, Cardiac, Renal, and Limb Defects Syndrome 3
56
6
Characteristics:OMIM:56
Inheritance:
autosomal recessive
Miscellaneous:
death in early infancy due to severe cardiac and renal anomalies Classifications: |
OMIM :
56
Vertebral, cardiac, renal, and limb defects syndrome-3 (VCRL3) is an autosomal recessive disorder characterized by severe cardiac and renal anomalies that are lethal in infancy, including hypoplastic or absent left ventricle, transposition of the great arteries, absent pulmonary trunk, and hypoplastic or absent kidneys. Patients also exhibit vertebral segmentation defects and shortening of the proximal long bones or micromelia (Szot et al., 2020).
For a discussion of genetic heterogeneity of VCRL, see VCRL1 (617660). (618845)
MalaCards based summary : Vertebral, Cardiac, Renal, and Limb Defects Syndrome 3, is also known as congenital nad deficiency disorder 3. An important gene associated with Vertebral, Cardiac, Renal, and Limb Defects Syndrome 3 is NADSYN1 (NAD Synthetase 1). Affiliated tissues include bone, kidney and cortex. |
Diseases in the Vertebral, Cardiac, Renal, and Limb Defects Syndrome 1 family:
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Symptoms via clinical synopsis from OMIM:56Clinical features from OMIM:618845 |
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MalaCards organs/tissues related to Vertebral, Cardiac, Renal, and Limb Defects Syndrome 3:40
Bone,
Kidney,
Cortex
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Articles related to Vertebral, Cardiac, Renal, and Limb Defects Syndrome 3:(showing 1, show less)
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ClinVar genetic disease variations for Vertebral, Cardiac, Renal, and Limb Defects Syndrome 3:6 (showing 4, show less)
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Search
GEO
for disease gene expression data for Vertebral, Cardiac, Renal, and Limb Defects Syndrome 3.
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