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Pediatric Disease Annotations & Medicines



   pellagra
  

Disease ID 931
Disease pellagra
Definition
A disease due to deficiency of NIACIN, a B-complex vitamin, or its precursor TRYPTOPHAN. It is characterized by scaly DERMATITIS which is often associated with DIARRHEA and DEMENTIA (the three D's).
Synonym
deficiencies niacin
deficiency niacin
niacin deficiency
niacin deficiency (disorder)
niacin deficiency
niacin deficiency pellagra
niacin-tryptophan deficiency
nicotinamide deficiency
nicotinic acid deficiency
pellagra (disorder)
pellagra [disease/finding]
pellagra disorder
pellagras
vitamin b3 deficiency
vitamin pp deficiency
Orphanet
DOID
UMLS
C0030783
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:15)
C0030783  |  pellagra  |  3
C0011603  |  dermatitis  |  3
C0030783  |  niacin deficiency  |  2
C0011991  |  diarrhea  |  2
C0024523  |  malabsorption syndrome  |  1
C0497327  |  dementia  |  1
C0024523  |  malabsorption  |  1
C1527336  |  sjogren's syndrome  |  1
C0030783  |  nicotinic acid deficiency  |  1
C0023801  |  lipomatosis  |  1
C0011570  |  depression  |  1
C0085642  |  livedo reticularis  |  1
C0043121  |  wernicke's encephalopathy  |  1
C0015230  |  rash  |  1
C0017675  |  glossitis  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:67)
2273  |  FHL1  |  DISEASES
23411  |  SIRT1  |  DISEASES
1666  |  DECR1  |  DISEASES
2936  |  GSR  |  DISEASES
7040  |  TGFB1  |  DISEASES
57817  |  HAMP  |  DISEASES
952  |  CD38  |  DISEASES
2597  |  GAPDH  |  DISEASES
10342  |  TFG  |  DISEASES
8997  |  KALRN  |  DISEASES
847  |  CAT  |  DISEASES
59272  |  ACE2  |  DISEASES
2694  |  GIF  |  DISEASES
642  |  BLMH  |  DISEASES
7305  |  TYROBP  |  DISEASES
3938  |  LCT  |  DISEASES
8942  |  KYNU  |  DISEASES
10190  |  TXNDC9  |  DISEASES
6523  |  SLC5A1  |  DISEASES
5226  |  PGD  |  DISEASES
4915  |  NTRK2  |  DISEASES
7082  |  TJP1  |  DISEASES
2071  |  ERCC3  |  DISEASES
9069  |  CLDN12  |  DISEASES
23498  |  HAAO  |  DISEASES
213  |  ALB  |  DISEASES
116842  |  LEAP2  |  DISEASES
4837  |  NNMT  |  DISEASES
5734  |  PTGER4  |  DISEASES
43  |  ACHE  |  DISEASES
340024  |  SLC6A19  |  DISEASES
660  |  BMX  |  DISEASES
24146  |  CLDN15  |  DISEASES
8685  |  MARCO  |  DISEASES
246329  |  STAC3  |  DISEASES
2520  |  GAST  |  DISEASES
2042  |  EPHA3  |  DISEASES
6731  |  SRP72  |  DISEASES
9536  |  PTGES  |  DISEASES
5498  |  PPOX  |  DISEASES
1811  |  SLC26A3  |  DISEASES
54716  |  SLC6A20  |  DISEASES
100506658  |  OCLN  |  DISEASES
7453  |  WARS  |  DISEASES
2073  |  ERCC5  |  DISEASES
130013  |  ACMSD  |  DISEASES
617  |  BCS1L  |  DISEASES
4638  |  MYLK  |  DISEASES
4536  |  MT-ND2  |  DISEASES
23038  |  WDTC1  |  DISEASES
8564  |  KMO  |  DISEASES
142  |  PARP1  |  DISEASES
8517  |  IKBKG  |  DISEASES
3654  |  IRAK1  |  DISEASES
4694  |  NDUFA1  |  DISEASES
27232  |  GNMT  |  DISEASES
54209  |  TREM2  |  DISEASES
353116  |  RILPL1  |  DISEASES
338442  |  HCAR2  |  DISEASES
1365  |  CLDN3  |  DISEASES
23475  |  QPRT  |  DISEASES
4780  |  NFE2L2  |  DISEASES
7086  |  TKT  |  DISEASES
3551  |  IKBKB  |  DISEASES
6510  |  SLC1A5  |  DISEASES
6999  |  TDO2  |  DISEASES
8914  |  TIMELESS  |  DISEASES
Locus(Waiting for update.)
Disease ID 931
Disease pellagra
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:10)
HP:0002014  |  Diarrhea  |  2
HP:0000992  |  Skin photosensitivity  |  2
HP:0001298  |  Encephalopathy  |  2
HP:0000988  |  Exanthem  |  1
HP:0000726  |  Dementia  |  1
HP:0001336  |  Myoclonic jerks  |  1
HP:0000206  |  Inflammation of the tongue  |  1
HP:0002024  |  Intestinal malabsorption  |  1
HP:0000716  |  Depression  |  1
HP:0000965  |  Livedo reticularis  |  1
Disease ID 931
Disease pellagra
Manually Symptom
UMLS  | Name(Total Manually Symptoms:17)
C1994997  |  intestinal symptoms
C1000483  |  anemia
C0752303  |  urological manifestations
C0730362  |  maculopathy
C0263556  |  tropical ulcer
C0262972  |  acute dermatitis
C0240182  |  leukonychia
C0233401  |  psychiatric symptoms
C0221505  |  cerebral lesions
C0155550  |  neural deafness
C0151467  |  addisonian crisis
C0042875  |  vitamin e deficiency
C0033975  |  psychosis
C0030499  |  parasitosis
C0027813  |  neuritis
C0019693  |  hiv infection
C0010346  |  crohn's disease
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)