Dihydropteridinereductasedeficiëntieziekte

Voorkeurslabel : Dihydropteridinereductasedeficiëntieziekte;

Obsolete resource : false;

Wikipedia automatic translation : Fenylketonurie;

Wikipedia link : https://nl.wikipedia.org/wiki/Fenylketonurie;

Details

Oorsprong id

D010661;

UMLS CUI

C0031485;

Automatic exact mappings (from CISMeF team)
- Hyperfenylalaninemie [MedDRA LLT]
- Hyperfenylalaninemie [MedDRA Preferred Term]
- Overige hyperfenylalaninemieën [ICD-10 Sub-category (who)]
- fenylpyruvaatoligofrenie [MedDRA LLT]
- tetrahydrobiopterine deficiëntie [MedDRA Preferred Term]
CISMeF manual mappings
- Deficiëntie van dihydrobiopteridinereductase [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Milde hyperfenylalaninemie [ORDO Disease]
- Neurometabole ziekte [ORDO Disease]
- Stoornis van het fenylalanine- of tyrosinemetabolisme [ORDO Disease]
- Stoornis van het neurotransmittermetabolisme en -transport [ORDO Disease]
- Stoornis van metabolisme van aminozuren en andere organische zuren [ORDO Disease]
ORDO relation(s)
- Fenylketonurie [ORDO Disease]
See also
- Urine [MeSH Descriptor]
UMLS correspondences (same concept)
- FKU [MedDRA LLT]
- Fenylketonurie [ORDO Disease]
- fenylalaninemie [MedDRA LLT]
- fenylalaninemie [MedDRA LLT]
- fenylketonurie [MedDRA Preferred Term]
- fenylketonurie (FKU) [MedDRA LLT]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

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