Acatalasia [akatalázie]
topical
3
- Terms
-
akatalasemie
akatalezemie
akatalezemie japonského typu
akatalezemie švýcarského typu
anenzymia catalasea
deficit katalázy
hypokatalasemie
hypokatalazemie
Takaharova nemoc
-
Acatalasemia
Acatalasemia Japanese Type
Acatalasemia Swiss Type
Catalase Deficiency
Hypocatalasemia
Hypocatalasia
Takahara Disease
Takahara's Disease
Persistent link
https://www.medvik.cz/link/D020642
Definition
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.
- DUI
- D020642 MeSH Browser
- CUI
- M0328366
- Previous indexing
- Catalase (1965-1999)
- History note
- 2000
- Public note
- 2000
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications
- DI
- diagnosis 1
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology 1
- EH
- ethnology
- ET
- etiology
- GE
- genetics
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology
- PP
- physiopathology 1
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy
- UR
- urine
- VE
- veterinary
- VI
- virology
...
Occurrences in Medvik records
C
Diseases
C16.320.565.663.265
Chondrodysplasia Punctata, Rhizomelic
C16.320.565.663.865
Refsum Disease, Infantile
C18.452.648.663.265
Chondrodysplasia Punctata, Rhizomelic
C18.452.648.663.865
Refsum Disease, Infantile