DiseaseID 3297
新生儿溶血性贫血
disease
NCI2016_02D:A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies.|MSH2017_2016_08_12:Hemolytic anemia due to various intrinsic defects of the erythrocyte
Relationship Network
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Disease: 1Symptom: 1Target: 12Links: 13
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 3297
- Core Entity Id
- 59486
- Source Entity Count
- 1
- Preferred Name
- Neonatal Hemolytic Anemia
- Name Cn
- 新生儿溶血性贫血
- Name Pinyin
- Xin Sheng Er Rong Xue Xing Pin Xue
- Name En
- Neonatal Hemolytic Anemia
- 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 Diseases
- Do Class
- disease of anatomical entity
- Hpo Class
- Abnormality of blood and blood-forming tissues
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
- Hpo Class Name
- Abnormality of blood and blood-forming tissues
- Do Class Name
- disease of anatomical entity
- Disease Definition
- NCI2016_02D:A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies.|MSH2017_2016_08_12:Hemolytic anemia due to various intrinsic defects of the erythrocyte.|HPO2016_07_04:A form of hemolytic anemia with congenital onset. [HPO:probinson]|CSP2006:includes hereditary erythrocyte membrane defects, enzyme deficiencies, hemoglobin abnormalities, stem cell defects (paroxysmal nocturnal hemoglobinuria), and alloimmune (Rh) disease of newborn.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Neonatal Hemolytic Anemia
Role
preferred
Name
Anemia, Hemolytic, Congenital
Role
preferred
Name
Congenital Haemolytic Anemia
Role
alias
Name
Congenital Hemolytic Anemia
Role
alias
Name
Hereditary Haemolytic Anaemia, Unspecified
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0004804
Herb
HBDIS000148HBDIS023497
Me Sh
D000745
Umls
C0002881
Icd10
D58.9
Sym Map
SMDE05848
Do Class
DOID:7
Dis Ge Net
C0002881C4020827
Umls Sty
T047
Hpo Class
HP:0001871
Me Sh Class
C15C16
Tcmbank Disease
202539868
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease of anatomical entity
Disease Type
disease
Hpo Class Name
Abnormality of blood and blood-forming tissues
Do Disease Class
disease of anatomical entity
Hpo Disease Class
Abnormality of blood and blood-forming tissues
Umls Disease Type
Disease or Syndrome
Disease Definition
NCI2016_02D:A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies.|MSH2017_2016_08_12:Hemolytic anemia due to various intrinsic defects of the erythrocyte.|HPO2016_07_04:A form of hemolytic anemia with congenital onset. [HPO:probinson]|CSP2006:includes hereditary erythrocyte membrane defects, enzyme deficiencies, hemoglobin abnormalities, stem cell defects (paroxysmal nocturnal hemoglobinuria), and alloimmune (Rh) disease of newborn.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or Syndrome