Vertebral, Cardiac, Renal, and Limb Defects Syndrome 3 (VCRL3)

Alias:
Vcrl3
Vertebral, Cardiac, Renal, and Limb Defects Syndrome, Type 3
Congenital Nad Deficiency Disorder 3
Congenital Nad Deficiency Disorder
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Vertebral, Cardiac, Renal, and Limb Defects Syndrome 3, also known as vcrl3, is related to congenital nad deficiency disorder and vertebral, cardiac, renal, and limb defects syndrome 1. An important gene associated with Vertebral, Cardiac, Renal, and Limb Defects Syndrome 3 is NADSYN1 (NAD Synthetase 1). Affiliated tissues include cortex and heart, and related phenotypes are sacral dimple and bicuspid aortic valve
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
4
3

Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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