DiseaseID 4682
肌红蛋白尿
disease
NCI2016_NICHD_1602D:The presence of myoglobin in the urine.|NCI2016_02D:The presence of myoglobin in the urine.|MSH2017_2016_08_12:The presence of MYOGLOBIN in URINE usually as a result of rhabdomyolysis.|HPO2016_07_04:P
Relationship Network
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Disease: 1Symptom: 7Target: 20Links: 31
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 4682
- Core Entity Id
- 61065
- Source Entity Count
- 1
- Preferred Name
- Myoglobinuria
- Name Cn
- 肌红蛋白尿
- Name Pinyin
- Ji Hong Dan Bai Niao
- Name En
- Myoglobinuria
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Musculoskeletal Diseases
- Do Class
- disease of anatomical entity
- Hpo Class
- Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system
- Mesh Class Name
- Musculoskeletal Diseases
- Hpo Class Name
- Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system
- Do Class Name
- disease of anatomical entity
- Disease Definition
- NCI2016_NICHD_1602D:The presence of myoglobin in the urine.|NCI2016_02D:The presence of myoglobin in the urine.|MSH2017_2016_08_12:The presence of MYOGLOBIN in URINE usually as a result of rhabdomyolysis.|HPO2016_07_04:Presence of myoglobin in the urine. [HPO:probinson]
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Myoglobinuria
Role
preferred
Name
Myoglobinuria, Acute Recurrent, Autosomal Recessive
Role
preferred
Name
Myoglobinuria, Recurrent
Role
preferred
Name
MYOGLOBINURIA, FAMILIAL PAROXYSMAL PARALYTIC
Role
alias
Name
Myoglobinuria, Episodic
Role
alias
Name
RHABDOMYOLYSIS, ACUTE RECURRENT
Role
alias
Name
Recurrent Myoglobinuria
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0002913HP:0003652
Herb
HBDIS002033HBDIS015719HBDIS016608
Me Sh
D009212
Omim
268200550500
Umls
C0027080C1849386
Icd10
R82.1
Sym Map
SMDE04293SMDE11243
Do Class
DOID:7
Dis Ge Net
C0027080C1838877C1849386
Umls Sty
T033T047
Hpo Class
HP:0000119HP:0001939
Me Sh Class
C05
Etcm Disease
Myoglobinuria, Acute Recurrent, Autosomal RecessiveMyoglobinuria, Recurrent
Tcmbank Disease
186792301296859516
Itcmdb Generated
ITX-DISEASE-2FCECD8CF429ITX-DISEASE-48AC4A509B55ITX-DISEASE-7AD0A1D185D5
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2v2
Suppress
0
Page Title
Disease Myoglobinuria, Acute Recurrent, Autosomal Recessive Details pageDisease Myoglobinuria, Recurrent Details page
Do Class Name
disease of anatomical entity
Disease Type
diseasephenotype
Hpo Class Name
Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system
Do Disease Class
disease of anatomical entity
Hpo Disease Class
Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system
Umls Disease Type
Disease or SyndromeFinding
Basic Information
Disease Name
Myoglobinuria, Acute Recurrent, Autosomal Recessive
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Bone diseases;Muscle diseases;Nephrological diseases;Neuronal diseases
Disease Name
Myoglobinuria, Recurrent
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Bone diseases;Muscle diseases;Nephrological diseases;Neuronal diseases
Disease Definition
NCI2016_NICHD_1602D:The presence of myoglobin in the urine.|NCI2016_02D:The presence of myoglobin in the urine.|MSH2017_2016_08_12:The presence of MYOGLOBIN in URINE usually as a result of rhabdomyolysis.|HPO2016_07_04:Presence of myoglobin in the urine. [HPO:probinson]
Me Sh Disease Class
Musculoskeletal Diseases
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Musculoskeletal Diseases
Umls Semantic Type Name
Disease or SyndromeFinding