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PedAM

Pediatric Disease Annotations & Medicines



   radioulnar synostosis
  

Disease ID 980
Disease radioulnar synostosis
Definition
An abnormal osseous union (fusion) between the radius and the ulna. [HPO:probinson]
Synonym
fused forearm bones
radioulnar synostosis (disorder)
synostosis radioulnar
OMIM
DOID
UMLS
C0158761
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:1)
C0040034  |  thrombocytopenia  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:42)
3207  |  HOXA11  |  DISEASES
11285  |  B4GALT7  |  DISEASES
57167  |  SALL4  |  DISEASES
1723  |  DHODH  |  DISEASES
3488  |  IGFBP5  |  DISEASES
9496  |  TBX4  |  DISEASES
3976  |  LIF  |  DISEASES
64131  |  XYLT1  |  DISEASES
3690  |  ITGB3  |  DISEASES
8455  |  ATRN  |  DISEASES
84162  |  KIAA1109  |  DISEASES
2122  |  MECOM  |  DISEASES
53834  |  FGFRL1  |  DISEASES
26229  |  B3GAT3  |  DISEASES
10262  |  SF3B4  |  DISEASES
23522  |  KAT6B  |  DISEASES
9965  |  FGF19  |  DISEASES
5648  |  MASP1  |  DISEASES
26585  |  GREM1  |  DISEASES
861  |  RUNX1  |  DISEASES
6910  |  TBX5  |  DISEASES
9241  |  NOG  |  DISEASES
9939  |  RBM8A  |  DISEASES
342184  |  FMN1  |  DISEASES
2261  |  FGFR3  |  DISEASES
26033  |  ATRNL1  |  DISEASES
4010  |  LMX1B  |  DISEASES
157680  |  VPS13B  |  DISEASES
1586  |  CYP17A1  |  DISEASES
10660  |  LBX1  |  DISEASES
860  |  RUNX2  |  DISEASES
4352  |  MPL  |  DISEASES
54880  |  BCOR  |  DISEASES
4038  |  LRP4  |  DISEASES
650  |  BMP2  |  DISEASES
126792  |  B3GALT6  |  DISEASES
6736  |  SRY  |  DISEASES
5744  |  PTHLH  |  DISEASES
9343  |  EFTUD2  |  DISEASES
2260  |  FGFR1  |  DISEASES
2263  |  FGFR2  |  DISEASES
3949  |  LDLR  |  DISEASES
Locus(Waiting for update.)
Disease ID 980
Disease radioulnar synostosis
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:3)
HP:0002974  |  Fused forearm bones
HP:0001377  |  Restricted elbow extension
HP:0003083  |  Dislocated radius
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:8)
Disease ID 980
Disease radioulnar synostosis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:1)
C1863881  |  tsukahara syndrome
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.)