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PedAM

Pediatric Disease Annotations & Medicines



   currarino triad
  

Disease ID 2000
Disease currarino triad
Synonym
currarino syndrome
currarino triad (disorder)
Orphanet
OMIM
UMLS
C1531773
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:1)
C0011991  |  diarrhea  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:2)
PCSK5  |  5125  |  CTD_human
MNX1  |  3110  |  CLINVAR;CTD_human;ORPHANET;UNIPROT
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus(Waiting for update.)
Disease ID 2000
Disease currarino triad
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:10)
HP:0000048  |  Bifid scrotum
HP:0002242  |  Abnormality of the intestine
HP:0100559  |  Lower limb asymmetry
HP:0008517  |  Aplasia/Hypoplasia of the sacrum
HP:0000047  |  Hypospadias
HP:0030736  |  Sacrococcygeal teratoma
HP:0000037  |  Male pseudohermaphroditism
HP:0000076  |  Vesicoureteral reflux
HP:0008736  |  Hypoplasia of penis
HP:0100026  |  Arteriovenous malformation
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:1)
HP:0002014  |  Diarrhea  |  1
Disease ID 2000
Disease currarino triad
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:1)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs121912547NA3110MNX1umls:C1531773CLINVARNA0.48434307NAMNX1;MNX1-AS17157009859GT
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.)