Coproporphyria, Hereditary [hereditární koproporfyrie]
topical
2
- Terms
-
HPC
koproporfyrie dědičná
-
Coproporphyrinogen Oxidase Deficiency
Hereditary Coproporphyria
Persistent link
https://www.medvik.cz/link/D046349
Definition
An autosomal dominant porphyria that is due to a deficiency of COPROPORPHYRINOGEN OXIDASE in the LIVER, the sixth enzyme in the 8-enzyme biosynthetic pathway of HEME. Clinical features include both neurological symptoms and cutaneous lesions. Patients excrete increased levels of porphyrin precursors, 5-AMINOLEVULINATE and COPROPORPHYRINS.
- DUI
- D046349 MeSH Browser
- CUI
- M0025971
- Previous indexing
- Porphyria (1965-2004); Porphyria, Hepatic (1993-2004)
- History note
- 2005; use PORPHYRIA, HEPATIC 1993-2004
- Public note
- 2005; see PORPHYRIA, HEPATIC 1993-2004
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications
- CN
- congenital
- DI
- diagnosis 1
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology
- GE
- genetics
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology
- PP
- physiopathology
- 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
Coproporphyria Disease MeSH Browser
Harderoporphyria Disease MeSH Browser