Descriptor English: | Acatalasia | ||||||
Descriptor Spanish: |
Acatalasia
| ||||||
Descriptor Portuguese: | Acatalasia | ||||||
Descriptor French: | Acatalasie | ||||||
Entry term(s): |
Acatalasemia Acatalasemia Japanese Type Acatalasemia Swiss Type Catalase Deficiencies Catalase Deficiency Deficiencies, Catalase Deficiency, Catalase Disease, Takahara Disease, Takahara's Hypocatalasemia Hypocatalasia Japanese Type, Acatalasemia Swiss Type, Acatalasemia Takahara Disease Takahara's Disease Takaharas Disease |
||||||
Tree number(s): |
C16.320.565.663.050 C18.452.648.663.050 |
||||||
RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D020642 | ||||||
Scope note: | 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. |
||||||
Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
||||||
Previous Indexing: |
Catalase (1965-1999) |
||||||
Public MeSH Note: | 2000 |
||||||
History Note: | 2000 |
||||||
DeCS ID: | 34377 | ||||||
Unique ID: | D020642 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 2000/01/01 | ||||||
Date of Entry: | 1999/11/03 | ||||||
Revision Date: | 2015/06/08 |
|
Acatalasia
- Preferred
Hypocatalasemia
- Narrower
Catalase Deficiency
- Related but not broader or narrower
Acatalasemia Japanese Type
- Narrower
Acatalasemia Swiss Type
- Narrower
Concept UI |
M0328366 |
Scope note | 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. |
Preferred term | Acatalasia |
Entry term(s) |
Acatalasemia Disease, Takahara Disease, Takahara's Takahara Disease Takahara's Disease Takaharas Disease |
Concept UI |
M0332925 |
Preferred term | Hypocatalasemia |
Entry term(s) |
Hypocatalasia |
Concept UI |
M0552965 |
Preferred term | Catalase Deficiency |
Entry term(s) |
Catalase Deficiencies Deficiencies, Catalase Deficiency, Catalase |
Concept UI |
M0552966 |
Preferred term | Acatalasemia Japanese Type |
Entry term(s) |
Japanese Type, Acatalasemia |
Concept UI |
M0552967 |
Preferred term | Acatalasemia Swiss Type |
Entry term(s) |
Swiss Type, Acatalasemia |
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey