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) |
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) HP:0003201 | Rhabdomyolysis | 10 HP:0000083 | Renal insufficiency | 10 HP:0001919 | Acute renal failure | 5 HP:0008682 | Renal tubular necrosis | 3 HP:0001324 | Muscular weakness | 2 HP:0003198 | Myopathic changes | 2 HP:0001903 | Anemia | 2 HP:0003326 | Muscle pain | 2 HP:0003394 | Muscle cramps | 2 HP:0003323 | Muscle weakness, progressive | 1 HP:0008942 | Rhabdomyolysis, acute | 1 HP:0012378 | Fatigue | 1 HP:0100614 | Muscle inflammation | 1 HP:0003202 | Neurogenic muscle atrophy, especially in the lower limbs | 1 HP:0003738 | Muscle pain on exercise | 1 |
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.) |