DiseaseID 4175
新生儿贫血
disease
MSH2017_2016_08_12:A condition characterized by the recurrence of HEMOGLOBINURIA caused by intravascular HEMOLYSIS. In cases occurring upon cold exposure (paroxysmal cold hemoglobinuria), usually after infections, there
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Symptom: 12Target: 12Links: 24
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 4175
- Core Entity Id
- 60484
- Source Entity Count
- 1
- Preferred Name
- Anemia, Neonatal
- Name Cn
- 新生儿贫血
- Name Pinyin
- Xin Sheng Er Pin Xue
- Name En
- Anemia, Neonatal
- 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 DiseasesImmune System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Hemic and Lymphatic DiseasesImmune System Diseases; Hemic and Lymphatic Diseases
- Do Class
- disease of anatomical entity
- Hpo Class
- Abnormality of metabolism/homeostasis; Abnormality of the genitourinary systemAbnormality of the immune system; Abnormality of blood and blood-forming tissues
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesHemic and Lymphatic DiseasesImmune System Diseases; Hemic and Lymphatic Diseases
- Hpo Class Name
- Abnormality of metabolism/homeostasis; Abnormality of the genitourinary systemAbnormality of the immune system; Abnormality of blood and blood-forming tissues
- Do Class Name
- disease of anatomical entity
- Disease Definition
- MSH2017_2016_08_12:A condition characterized by the recurrence of HEMOGLOBINURIA caused by intravascular HEMOLYSIS. In cases occurring upon cold exposure (paroxysmal cold hemoglobinuria), usually after infections, there is a circulating antibody which is also a cold hemolysin. In cases occurring during or after sleep (paroxysmal nocturnal hemoglobinuria), the clonal hematopoietic stem cells exhibit a global deficiency of cell membrane proteins.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Anemia, Neonatal
Role
preferred
Name
Cold Hemagglutinin Disease
Role
preferred
Name
Cold Hemoglobinuria
Role
preferred
Name
Erythroblastosis, Fetal
Role
preferred
Name
Hemoglobinuria, Paroxysmal
Role
preferred
Name
Paroxysmal Nocturnal Hemoglobinuria
Role
preferred
Name
Paroxysmal Nocturnal Hemoglobinuria 1
Role
preferred
Name
Paroxysmal Nocturnal Hemoglobinuria 2
Role
preferred
Name
Anemia, Hemolytic, Idiopathic Acquired
Role
preferred
Name
Autoimmune Hemolytic Anemia
Role
preferred
Name
Cold Paroxysmal Hemoglobinuria
Role
preferred
Name
Idiopathic Autoimmune Hemolytic Anemia
Role
preferred
Name
Anemia, Autoimmune Hemolytic
Role
alias
Name
Anemia, Hemolytic, Autoimmune
Role
alias
Name
Autoimmune Haemolytic Anaemia
Role
alias
Name
Cold Agglutinin Disease
Role
alias
Name
Fetal Erythroblastosis
Role
alias
Name
Haemolytic Disease of Fetus And Newborn
Role
alias
Name
Haemolytic Disease of Fetus And Newborn, Unspecified
Role
alias
Name
Hemolytic Anemia, Autoimmune
Role
alias
Name
Marchiafava-Micheli Disease
Role
alias
Name
Neonatal Anemia
Role
alias
Name
Nocturnal Paroxysmal Hemoglobinuria
Role
alias
Name
PNH
Role
alias
Name
PNH1
Role
alias
Name
PNH2
Role
alias
Name
Paroxysmal Hemoglobinuria, Cold
Role
alias
Name
Paroxysmal Nocturnal Haemoglobinuria
Role
alias
Name
Paroxysmal Nocturnal Haemoglobinuria [Marchiafava-Micheli]
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0001890HP:0004818
Herb
HBDIS000147HBDIS000150HBDIS000156HBDIS000977HBDIS001310HBDIS001857HBDIS003431HBDIS004194HBDIS010028HBDIS022237HBDIS029481
Me Sh
D000744D000751D004899D006457
Omim
205700300818615399
Umls
C0002880C0014761C0019050C0024790C0086774C0175816C3806670C3809369
Icd10
D59.1D59.5D59.6P55P55.9
Med Dra
10034042
Sym Map
SMDE01871SMDE03755SMDE04304SMDE06193SMDE07307SMDE07308SMDE08481SMDE09331
Do Class
DOID:7
Dis Ge Net
C0002880C0002883C0002891C0014761C0019050C0024790C0086774C0175816C0543663C3806670C3809369
Orphanet
447
Umls Sty
T047
Hpo Class
HP:0000119HP:0001871HP:0001939HP:0002715
Me Sh Class
C13C15C16C20
Tcmbank Disease
157381739917520181542063223288244025871681672839323941
Itcmdb Generated
ITX-DISEASE-2D0B5E8DC280ITX-DISEASE-6680D512A620ITX-DISEASE-7EF4056EA936ITX-DISEASE-E55222CE0581
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v1,v2v2
Suppress
0
Do Class Name
disease of anatomical entity
Disease Type
disease
Hpo Class Name
Abnormality of metabolism/homeostasis; Abnormality of the genitourinary systemAbnormality of the immune system; Abnormality of blood and blood-forming tissues
Do Disease Class
disease of anatomical entity
Hpo Disease Class
Abnormality of metabolism/homeostasis; Abnormality of the genitourinary systemAbnormality of the immune system; Abnormality of blood and blood-forming tissues
Umls Disease Type
Disease or Syndrome
Disease Definition
MSH2017_2016_08_12:A condition characterized by the recurrence of HEMOGLOBINURIA caused by intravascular HEMOLYSIS. In cases occurring upon cold exposure (paroxysmal cold hemoglobinuria), usually after infections, there is a circulating antibody which is also a cold hemolysin. In cases occurring during or after sleep (paroxysmal nocturnal hemoglobinuria), the clonal hematopoietic stem cells exhibit a global deficiency of cell membrane proteins.NCI2016_NCI-GLOSS_1602D:A condition in which the body's immune system stops red blood cells from forming or causes them to clump together. Autoimmune hemolytic anemia can occur in patients who have chronic lymphocytic leukemia (CLL).|NCI2016_02D:An acquired anemia caused by destruction of the red blood cells by autoantibodies. Causes include autoimmune disorders, lymphoproliferative disorders, and infections.|MSH2017_2016_08_12:Acquired hemolytic anemia due to the presence of AUTOANTIBODIES which agglutinate or lyse the patient's own RED BLOOD CELLS.|HPO2016_07_04:An autoimmune form of hemolytic anemia. [HPO:probinson]|CSP2006:due to acquired antierythrocyte autoantibodies causing premature erythrocyte clearance by the spleen; antibodies can be warm or cold active; usually slow developing and treatable.NCI2016_NICHD_1602D:A condition of the newborn characterized by the destruction of red blood cells initiated by the transmission of IgG antibodies from mother to child via the placenta.|NCI2016_02D:A disorder of the fetus or newborn that occurs when fetal cells that are coated with IgG alloantibodies from the mother attack antigens inherited from the father. Severity can range from absence of symptoms to death.|MSH2017_2016_08_12:A condition characterized by the abnormal presence of ERYTHROBLASTS in the circulation of the FETUS or NEWBORNS. It is a disorder due to BLOOD GROUP INCOMPATIBILITY, such as the maternal alloimmunization by fetal antigen RH FACTORS leading to HEMOLYSIS of ERYTHROCYTES, hemolytic anemia (ANEMIA, HEMOLYTIC), general edema (HYDROPS FETALIS), and SEVERE JAUNDICE IN NEWBORN.|CSP2006:hemolytic anemia of the fetus or newborn caused by transplacental transmission of maternally formed antibody, usually secondary to an incompatibility between the blood groups of mother and offspring.Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal hematopoietic stem cell disorder characterized by corpuscular hemolytic anemia, bone marrow failure and frequent thrombotic events.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesHemic and Lymphatic DiseasesImmune System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Hemic and Lymphatic DiseasesImmune System Diseases; Hemic and Lymphatic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesHemic and Lymphatic DiseasesImmune System Diseases; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or Syndrome