DiseaseID 5811
红细胞增多症
disease
NCI2016_NICHD_1602D:Abnormally high mass or concentration of red blood cells in the blood, either due to an increase in erythropoiesis or a decrease in plasma volume.|NCI2016_02D:Abnormally high mass or concentration of
Relationship Network
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Disease: 1Herb: 12Symptom: 12Target: 24Links: 48
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 5811
- Core Entity Id
- 62370
- Source Entity Count
- 1
- Preferred Name
- Polyglobulia
- Name Cn
- 红细胞增多症
- Name Pinyin
- Hong Xi Bao Zeng Duo Zheng
- Name En
- Polyglobulia
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesHemic and Lymphatic DiseasesNeoplasms; Hemic and Lymphatic Diseases
- Do Class
- disease of anatomical entity; genetic disease
- Hpo Class
- Abnormality of blood and blood-forming tissues
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesHemic and Lymphatic DiseasesNeoplasms; Hemic and Lymphatic Diseases
- Hpo Class Name
- Abnormality of blood and blood-forming tissues
- Do Class Name
- genetic disease; disease of anatomical entity
- Disease Definition
- NCI2016_NICHD_1602D:Abnormally high mass or concentration of red blood cells in the blood, either due to an increase in erythropoiesis or a decrease in plasma volume.|NCI2016_02D:Abnormally high mass or concentration of red blood cells in the blood, either due to an increase in erythropoiesis or a decrease in plasma volume.(NICHD)|MSH2017_2016_08_12:An increase in the total red cell mass of the blood. (Dorland, 27th ed)|HPO2016_07_04:Polycythemia is diagnosed if the red blood cell count, the hemoglobin level, and the red blood cell volume all exceed the upper limits of normal. [HPO:probinson]|CSP2006:increase in the total red cell mass of the blood.|CHV2011_02:an abnormal increase of the red blood cell in the circulating blood|CHV2011_02:an abnormal increase of the red blood cell in the circulating blood
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Polyglobulia
Role
preferred
Name
Erythrocytosis, Familial, 1
Role
preferred
Name
Erythrocytosis, Familial, 2
Role
preferred
Name
Polycythemia
Role
preferred
Name
Primary Familial Polycythemia
Role
preferred
Name
Secondary Polycythemia
Role
preferred
Name
Erythrocytosis
Role
preferred
Name
Erythrocytosis Due To Tissue Hypoxemia
Role
preferred
Name
Erythrocytosis Familial, 1
Role
preferred
Name
Familial Erythrocytosis
Role
preferred
Name
Polycythemia Due To Erythropoietin
Role
preferred
Name
Polycythemia Due To Excess Erythopoetin Production
Role
preferred
Name
Polycythemia Due To Fall In Plasma Volume
Role
preferred
Name
Polycythemia Due To High Altitude
Role
preferred
Name
Polycythemia Due To Stress
Role
preferred
Name
Relative Erythrocytosis
Role
preferred
Name
Stress Polycythemia
Role
preferred
Name
Abnormally Shaped Erythrocytes
Role
alias
Name
Acquired Polycythemia
Role
alias
Name
Congenital Erythrocytosis Due To Erythropoietin Receptor
Role
alias
Name
Congenital Polycythemia Due To Erythropoietin Receptor Mutation
Role
alias
Name
ECYT1
Role
alias
Name
ECYT2
Role
alias
Name
ERYTHROCYTOSIS, AUTOSOMAL DOMINANT BENIGN
Role
alias
Name
ERYTHROCYTOSIS, AUTOSOMAL RECESSIVE BENIGN
Role
alias
Name
Erythropoietin Polycythemia
Role
alias
Name
Familial Erythrocytosis 1
Role
alias
Name
Familial Erythrocytosis 2
Role
alias
Name
PFCP
Role
alias
Name
POLYCYTHEMIA, CHUVASH TYPE
Role
alias
Name
POLYCYTHEMIA, PRIMARY FAMILIAL AND CONGENITAL
Role
alias
Name
POLYCYTHEMIA, VHL-DEPENDENT
Role
alias
Name
Primary Congenital Erythrocytosis
Role
alias
Name
Primary Familial And Congenital Polycythemia
Role
alias
Name
Primary Polycythemia
Role
alias
Name
Secondary Polycythaemia
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS002436HBDIS003711HBDIS004622HBDIS006722HBDIS008587HBDIS009993HBDIS012231HBDIS012232HBDIS013476HBDIS014470HBDIS015638HBDIS018492HBDIS020063HBDIS020064HBDIS027270
Omim
133100
Umls
C0152264C1318533C1837915
Icd10
D75.0
Sym Map
SMDE02608SMDE03433SMDE05053SMDE12277SMDE13024
Do Class
DOID:630DOID:7
Dis Ge Net
C0032461C0152264C0221276C0272144C0391869C0541719C0865275C0865276C1318533C1527405C1837915C1868945C2873823C2873824C4551637
Orphanet
90042
Umls Sty
T033T047
Hpo Class
HP:0001871
Me Sh Class
C04C15C16
Etcm Disease
Erythrocytosis, Familial, 1Erythrocytosis, Familial, 2
Tcmbank Disease
11731319215559155611576418361186251972622338245712938030079306773149563187646
Itcmdb Generated
ITX-DISEASE-32D9E544C4E9ITX-DISEASE-D573985BEE41ITX-DISEASE-EC1807111B49
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2v2
Suppress
01
Page Title
Disease Erythrocytosis, Familial, 1 Details pageDisease Erythrocytosis, Familial, 2 Details page
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
diseasephenotype
Hpo Class Name
Abnormality of blood and blood-forming tissues
Link Disease Id
3433.0
Do Disease Class
disease of anatomical entity; genetic disease
Hpo Disease Class
Abnormality of blood and blood-forming tissues
Umls Disease Type
Disease or SyndromeFinding
Basic Information
Disease Name
Erythrocytosis, Familial, 1
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Blood diseases;Immune diseases
Disease Name
Erythrocytosis, Familial, 2
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Blood diseases;Immune diseases
Disease Definition
NCI2016_NICHD_1602D:Abnormally high mass or concentration of red blood cells in the blood, either due to an increase in erythropoiesis or a decrease in plasma volume.|NCI2016_02D:Abnormally high mass or concentration of red blood cells in the blood, either due to an increase in erythropoiesis or a decrease in plasma volume.(NICHD)|MSH2017_2016_08_12:An increase in the total red cell mass of the blood. (Dorland, 27th ed)|HPO2016_07_04:Polycythemia is diagnosed if the red blood cell count, the hemoglobin level, and the red blood cell volume all exceed the upper limits of normal. [HPO:probinson]|CSP2006:increase in the total red cell mass of the blood.|CHV2011_02:an abnormal increase of the red blood cell in the circulating blood|CHV2011_02:an abnormal increase of the red blood cell in the circulating bloodPrimary familial polycythemia is an inherited hematological disorder resulting from mutations in the erythropoietin (EPO) receptor and is characterized by an elevated absolute red blood cell mass caus
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesHemic and Lymphatic DiseasesNeoplasms; Hemic and Lymphatic Diseases
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesHemic and Lymphatic DiseasesNeoplasms; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or SyndromeFinding