MeSH Browser

MeSH Heading: Anemia, Dyserythropoietic, Congenital
Tree Number(s): C15.378.050.141.150.095; C16.320.070.095
Unique ID: D000742
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D000742
Scope Note: A familial disorder characterized by ANEMIA with multinuclear ERYTHROBLASTS, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors (ERYTHROID PRECURSOR CELLS). Type II is the most common of the 3 types; it is often referred to as HEMPAS, based on the Hereditary Erythroblast Multinuclearity with Positive Acidified Serum test.
Entry Version: ANEMIA DYSERYTHROPOIETIC CONGEN
Entry Term(s): Anemia With Multinucleated Erythroblasts; Anemia, Congenital Dyserythropoietic; Anemia, Congenital Dyserythropoietic, Type II; Anemia, Dyserythropoietic Congenital, Type I; Anemia, Dyserythropoietic Congenital, Type II; Anemia, Dyserythropoietic Congenital, Type III; Anemia, Dyserythropoietic, Congenital Type 1; Anemia, Dyserythropoietic, Congenital Type 2; Anemia, Dyserythropoietic, Congenital, Type I; Anemia, Dyserythropoietic, Congenital, Type II; Anemia, Dyserythropoietic, Congenital, Type III; Congenital Dyserythropoietic Anemia; Congenital Dyserythropoietic Anemia Type 1; Congenital Dyserythropoietic Anemia Type II; Congenital Dyserythropoietic Anemia, Type I; Congenital Dyserythropoietic Anemia, Type III; Dyserythropoietic Anemia, Congenital; Dyserythropoietic Anemia, Congenital Type 1; Dyserythropoietic Anemia, Congenital Type 2; Dyserythropoietic Anemia, Congenital, Type I; Dyserythropoietic Anemia, Congenital, Type II; Dyserythropoietic Anemia, Congenital, Type III; Dyserythropoietic Anemia, HEMPAS Type; HEMPAS; HEMPAS Anemia; Hereditary Erythroblast Multinuclearity with Positive Acidified Serum; Hereditary Erythroblastic Multinuclearity with Positive Acidified-Serum Test; Type I Congenital Dyserythropoietic Anemia
Previous Indexing: Anemia (1966-1979); Erythropoiesis (1966-1979)
Public MeSH Note: 1991; see ANEMIA, HEMOLYTIC, CONGENITAL 1980-1990
History Note: 1991(1980); use ANEMIA, HEMOLYTIC, CONGENITAL 1980-1990
Date Established: 1991/01/01
Date of Entry: 1979/04/23
Revision Date: 2023/02/26

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Hemic and Lymphatic Diseases [C15]
- Hematologic Diseases [C15.378]
  - Anemia [C15.378.050]
    - Anemia, Hemolytic [C15.378.050.141]
      - Anemia, Hemolytic, Congenital [C15.378.050.141.150]
        
        Anemia, Dyserythropoietic, Congenital [C15.378.050.141.150.095]
        
        Anemia, Hemolytic, Congenital Nonspherocytic [C15.378.050.141.150.100]
        
        Anemia, Sickle Cell [C15.378.050.141.150.150]
        
        Elliptocytosis, Hereditary [C15.378.050.141.150.365]
        
        Glucosephosphate Dehydrogenase Deficiency [C15.378.050.141.150.480]
        
        Hemoglobin C Disease [C15.378.050.141.150.490]
        
        Spherocytosis, Hereditary [C15.378.050.141.150.785]
        
        Thalassemia [C15.378.050.141.150.875]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
  - Anemia, Hemolytic, Congenital [C16.320.070]

Anemia, Dyserythropoietic, Congenital Preferred

Concept UI: M0001122
Scope Note: A familial disorder characterized by ANEMIA with multinuclear ERYTHROBLASTS, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors (ERYTHROID PRECURSOR CELLS). Type II is the most common of the 3 types; it is often referred to as HEMPAS, based on the Hereditary Erythroblast Multinuclearity with Positive Acidified Serum test.
Terms: Anemia, Dyserythropoietic, Congenital Preferred Term
Term UI T002215
Date01/01/1999
LexicalTag NON
ThesaurusID; Dyserythropoietic Anemia, Congenital
Term UI T002214
Date04/23/1979
LexicalTag NON
ThesaurusID UNK (19XX); Anemia, Congenital Dyserythropoietic
Term UI T002212
Date04/23/1979
LexicalTag NON
ThesaurusID UNK (19XX); Congenital Dyserythropoietic Anemia
Term UI T002213
Date04/23/1979
LexicalTag NON
ThesaurusID

Anemia, Dyserythropoietic, Congenital, Type II Narrower

Anemia, Dyserythropoietic, Congenital, Type III Narrower

Anemia, Dyserythropoietic, Congenital, Type I Narrower

Anemia, Dyserythropoietic, Congenital MeSH Descriptor Data 2024