KEGG   DISEASE: Vertebral, cardiac, renal, and limb defects syndrome
Entry
H02087                      Disease                                
Name
Vertebral, cardiac, renal, and limb defects syndrome;
Congenital NAD deficiency disorder
Description
Vertebral, cardiac, renal, and limb defects syndrome (VCRL) is an autosomal recessive congenital malformation syndrome. It has been reported that disruption of nicotinamide adenine dinucleotide (NAD) synthesis causes a deficiency of NAD and congenital malformations in humans and mice.
Category
Inherited metabolic disorder
Brite
Human diseases in ICD-11 classification [BR:br08403]
 20 Developmental anomalies
  Multiple developmental anomalies or syndromes
   LD2F  Syndromes with multiple structural anomalies, without predominant body system involvement
    H02087  Vertebral, cardiac, renal, and limb defects syndrome
Pathway-based classification of diseases [BR:br08402]
 Amino acid metabolism
  nt06036  Lysine degradation
   H02087  Vertebral, cardiac, renal, and limb defects syndrome
Pathway
hsa01240  Biosynthesis of cofactors
hsa00380  Tryptophan metabolism
Network
nt06036 Lysine degradation
Gene
(VCRL1) HAAO [HSA:23498] [KO:K00452]
(VCRL2) KYNU [HSA:8942] [KO:K01556]
(VCRL3) NADSYN1 [HSA:55191] [KO:K01950]
Other DBs
ICD-11: LD2F.1Y
OMIM: 617660 617661 618845
Reference
PMID:28792876 (HAAO KYNU)
  Authors
Shi H, Enriquez A, Rapadas M, Martin EMMA, Wang R, Moreau J, Lim CK, Szot JO, Ip E, Hughes JN, Sugimoto K, Humphreys DT, McInerney-Leo AM, Leo PJ, Maghzal GJ, Halliday J, Smith J, Colley A, Mark PR, Collins F, Sillence DO, Winlaw DS, Ho JWK, Guillemin GJ, Brown MA, Kikuchi K, Thomas PQ, Stocker R, Giannoulatou E, Chapman G, Duncan EL, Sparrow DB, Dunwoodie SL
  Title
NAD Deficiency, Congenital Malformations, and Niacin Supplementation.
  Journal
N Engl J Med 377:544-552 (2017)
DOI:10.1056/NEJMoa1616361
Reference
PMID:31883644 (NADSYN1)
  Authors
Szot JO, Campagnolo C, Cao Y, Iyer KR, Cuny H, Drysdale T, Flores-Daboub JA, Bi W, Westerfield L, Liu P, Leung TN, Choy KW, Chapman G, Xiao R, Siu VM, Dunwoodie SL
  Title
Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency Disorders.
  Journal
Am J Hum Genet 106:129-136 (2020)
DOI:10.1016/j.ajhg.2019.12.006
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