Home Contact Sitemap

eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   myoglobinuria
  

Disease ID 1480
Disease myoglobinuria
Definition
The presence of MYOGLOBIN in URINE usually as a result of rhabdomyolysis.
Synonym
[d]myoglobinuria
[d]myoglobinuria (context-dependent category)
[d]myoglobinuria (situation)
myoglobinuria (finding)
myoglobinuria [disease/finding]
myoglobinurias
DOID
ICD10
UMLS
C0027080
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:12)
C0035078  |  renal failure  |  7
C0022660  |  acute renal failure  |  4
C0022672  |  acute tubular necrosis  |  3
C0021400  |  influenza  |  2
C0026848  |  myopathy  |  2
C0042769  |  virus infection  |  1
C0011881  |  diabetic nephropathy  |  1
C0002871  |  anaemia  |  1
C1565489  |  renal insufficiency  |  1
C0002871  |  anemia  |  1
C1565662  |  acute renal insufficiency  |  1
C0024530  |  malaria  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
3939  |  LDHA  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:48)
26090  |  ABHD12  |  2.348  |  DISEASES
37  |  ACADVL  |  5.036  |  DISEASES
224  |  ALDH3A2  |  1.591  |  DISEASES
226  |  ALDOA  |  1.788  |  DISEASES
270  |  AMPD1  |  3.953  |  DISEASES
54840  |  APTX  |  1.574  |  DISEASES
567  |  B2M  |  1.007  |  DISEASES
820  |  CAMP  |  2.332  |  DISEASES
825  |  CAPN3  |  1.177  |  DISEASES
859  |  CAV3  |  1.114  |  DISEASES
548596  |  CKMT1A  |  1.655  |  DISEASES
1376  |  CPT2  |  5.382  |  DISEASES
8029  |  CUBN  |  1.346  |  DISEASES
1576  |  CYP3A4  |  1.055  |  DISEASES
1756  |  DMD  |  3.414  |  DISEASES
2027  |  ENO3  |  1.803  |  DISEASES
2104  |  ESRRG  |  1.725  |  DISEASES
2110  |  ETFDH  |  3.031  |  DISEASES
79147  |  FKRP  |  2.366  |  DISEASES
2632  |  GBE1  |  3.323  |  DISEASES
2805  |  GOT1  |  2.125  |  DISEASES
3033  |  HADH  |  1.416  |  DISEASES
3030  |  HADHA  |  2.129  |  DISEASES
3032  |  HADHB  |  3.45  |  DISEASES
100124700  |  HOTAIR  |  2.07  |  DISEASES
102723508  |  KANTR  |  1.057  |  DISEASES
3939  |  LDHA  |  3.219  |  DISEASES
64900  |  LPIN3  |  2.709  |  DISEASES
4151  |  MB  |  6.82  |  DISEASES
92399  |  MRRF  |  2.016  |  DISEASES
4512  |  MT-CO1  |  2.447  |  DISEASES
4513  |  MT-CO2  |  2.876  |  DISEASES
4514  |  MT-CO3  |  1.254  |  DISEASES
4519  |  MT-CYB  |  2.802  |  DISEASES
4535  |  MT-ND1  |  1.562  |  DISEASES
23590  |  PDSS1  |  2.413  |  DISEASES
57107  |  PDSS2  |  2.457  |  DISEASES
5213  |  PFKM  |  4.664  |  DISEASES
5214  |  PFKP  |  2.03  |  DISEASES
5230  |  PGK1  |  3.212  |  DISEASES
10908  |  PNPLA6  |  1.169  |  DISEASES
6261  |  RYR1  |  1.935  |  DISEASES
6342  |  SCP2  |  1.881  |  DISEASES
10500  |  SEMA6C  |  1.471  |  DISEASES
116085  |  SLC22A12  |  1.359  |  DISEASES
6625  |  SNRNP70  |  1.682  |  DISEASES
7137  |  TNNI3  |  2.006  |  DISEASES
23038  |  WDTC1  |  1.094  |  DISEASES
Locus(Waiting for update.)
Disease ID 1480
Disease myoglobinuria
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:15)
Disease ID 1480
Disease myoglobinuria
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total 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.)
Disease ID 1480
Disease myoglobinuria
Case(Waiting for update.)