elliptocytosis, hereditary

Preferred Label : elliptocytosis, hereditary;

MeSH definition : An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape.;

MeSH synonym : ovalocytosis, hereditary; hereditary ovalocytosis; hereditary elliptocytoses; hereditary ovalocytoses; ovalocytoses, hereditary; elliptocytoses, hereditary; hereditary elliptocytosis;

MeSH annotation : a congen hemolytic anemia; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES;

Wikipedia link : https://en.wikipedia.org/wiki/Hereditary elliptocytosis;

Details

Origin ID

D004612;

UMLS CUI

C0013902;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Hereditary elliptocytosis [PASCAL descriptor]
- Southeast Asian ovalocytosis [ORDO Disease]
Currated CISMeF NLP mapping
- Congenital elliptocytosis (disorder) [SNOMED CT concept]
- Elliptocytosis [HPO term]
- Elliptocytosis hereditary [MedDRA Preferred Term]
- Hereditary Elliptocytosis [NCIt concept]
- Hereditary elliptocytosis [ICD-10 Sub-category]
- Hereditary elliptocytosis [ICD-11 Subcategory]
- Hereditary elliptocytosis [ICD-10 Sub-category (who)]
- Hereditary elliptocytosis [ICD-9 code]
- Hereditary elliptocytosis [ORDO Disease]
- Hereditary elliptocytosis [MedDRA LLT]
- Hereditary elliptocytosis (disorder) [SNOMED CT concept]
- hereditary elliptocytosis [DO Concept]
- hereditary elliptocytosis, nos [SNOMED Notion]
DO Cross reference
- hereditary elliptocytosis [DO Concept]
False automatic mappings
- Congenital elliptocytosis (disorder) [SNOMED CT concept]
HPO term
- Elliptocytosis [HPO term]
Indexing information
- spectrin, sp alpha(I-65)- [MeSH Supplementary Concept]
ORDO relation(s)
- Hereditary elliptocytosis [ORDO Disease]
Record concept(s)
- elliptocytosis, hereditary [MeSH concept]
Related MeSH Supplementary Concept(s)
- alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis [MeSH Supplementary Concept]
- elliptocytosis 1 [MeSH Supplementary Concept]
- elliptocytosis 2 [MeSH Supplementary Concept]
- elliptocytosis 3 [MeSH Supplementary Concept]
- elliptocytosis 4 [MeSH Supplementary Concept]
- elliptocytosis, atypical [MeSH Supplementary Concept]
- glyoxalase II deficiency [MeSH Supplementary Concept]
- ovalocytosis, Malaysian-Melanesian-Filipino type [MeSH Supplementary Concept]
- ovalocytosis, hereditary hemolytic [MeSH Supplementary Concept]
- ovalocytosis, hereditary hemolytic, with defective erythropoiesis [MeSH Supplementary Concept]
- pyropoikilocytosis, hereditary [MeSH Supplementary Concept]
See also
- anemia, sideroblastic [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital elliptocytosis (disorder) [SNOMED CT concept]
- Elliptocytosis hereditary [MedDRA Preferred Term]
- Hereditary Elliptocytosis [NCIt concept]
- Hereditary elliptocytosis [ORDO Disease]
- Hereditary elliptocytosis [ICD-9 code]
- Hereditary elliptocytosis [ICD-10 Sub-category (who)]
- Hereditary elliptocytosis [ICD-10 Sub-category]
- Hereditary elliptocytosis [ICD-11 Subcategory]
- Hereditary elliptocytosis [MedDRA LLT]
- Hereditary elliptocytosis (disorder) [SNOMED CT concept]
- hereditary elliptocytosis [DO Concept]
- hereditary elliptocytosis, nos [SNOMED Notion]
Validated automatic mappings to NTBT
- elliptocytosis [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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