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PedAM

Pediatric Disease Annotations & Medicines



   sacrococcygeal teratoma
  

Disease ID 1371
Disease sacrococcygeal teratoma
Definition
A teratoma that is found at the base of the coccyx. It is the most commonly seen tumor in newborns.
Synonym
altman type iv sacrococcygeal teratoma
pre-sacral teratoma
presacral teratoma
retrorectal teratoma
sacrococcygeal teratoma (disorder)
teratoma sacrococcygeal
UMLS
C0559459
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:7)
C0020305  |  fetal hydrops  |  2
C0027819  |  neuroblastoma  |  1
C0039538  |  teratoma  |  1
C0018801  |  cardiac failure  |  1
C0022660  |  acute renal failure  |  1
C0035078  |  renal failure  |  1
C0265706  |  gastroschisis  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus(Waiting for update.)
Disease ID 1371
Disease sacrococcygeal teratoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:11)
HP:0002664  |  Neoplasia  |  2
HP:0000078  |  Genital abnormalities  |  2
HP:0000119  |  Genitourinary abnormality  |  2
HP:0001919  |  Acute renal failure  |  1
HP:0003006  |  Neuroblastoma  |  1
HP:0001518  |  Small for gestational age  |  1
HP:0009792  |  Teratoma  |  1
HP:0001695  |  Cardiac arrest  |  1
HP:0000083  |  Renal insufficiency  |  1
HP:0001635  |  Congestive heart failure  |  1
HP:0001543  |  Gastroschisis  |  1
Disease ID 1371
Disease sacrococcygeal teratoma
Manually Symptom
UMLS  | Name(Total Manually Symptoms:4)
C2609079  |  mirror syndrome
C0752303  |  urological manifestations
C0206659  |  embryonal adenocarcinoma
C0010481  |  cushing syndrome
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:1)
C2609079  |  mirror syndrome  |  1
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:1)
HP ID HP Name MP ID MP Name Annotation
HP:0001578HypercortisolismMP:0002420abnormal adaptive immunity;
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.)