Structured Summary
Abstract
A rare autosomal recessive disorder resulting from the absence of CATALASE activity. Though usually asymptomatic, a syndrome of oral ulcerations and gangrene may be present.
MeSH Record
Classification
Broader headings
Related Concepts
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MeSH Record
Synonyms
16 entry terms
- Acatalasemia
- Takahara Disease
- Takahara's Disease
- Disease, Takahara
- Disease, Takahara's
- Takaharas Disease
- Acatalasemia Japanese Type
- Acatalasemia Swiss Type
- Catalase Deficiency
- Hypocatalasemia
- Hypocatalasia
- Catalase Deficiencies
- Deficiencies, Catalase
- Deficiency, Catalase
- Japanese Type, Acatalasemia
- Swiss Type, Acatalasemia
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2000
MeSH Record
Previous Indexing
- Catalase (1965-1999)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Acatalasia. Medical Subject Headings (MeSH). 2026. Unique ID D020642. http://id.nlm.nih.gov/mesh/2026/D020642
- Acatalasia. In: Wikipedia. https://en.wikipedia.org/wiki/Acatalasia
- Acatalasia. In: Wikidata. https://www.wikidata.org/wiki/Q3273331