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Descriptor English: Keratin-4
Descriptor Spanish: Queratina-4
Descriptor queratina-4
Entry term(s) queratina 4
Scope note: Queratina de tipo II que se encuentra en asociación con la QUERATINA 13 en el EPITELIO estratificado interno. Los defectos del gen de la queratina 4 son una causa de LEUCOQUERATOSIS MUCOSA HEREDITARIA.
Descriptor Portuguese: Queratina-4
Descriptor French: Kératine-4
Entry term(s): Cytokeratin 4
Cytokeratin-4
Keratin 4
Tree number(s): D05.750.078.593.450.600.400
D12.776.220.475.450.600.400
D12.776.860.607.650.400
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D053527
Scope note: A type II keratin that is found associated with the KERATIN-13 in the internal stratified EPITHELIUM. Defects in gene for keratin-4 are a cause of HEREDITARY MUCOSAL LEUKOKERATOSIS.
Allowable Qualifiers: AD administration & dosage
AE adverse effects
AG agonists
AI antagonists & inhibitors
AN analysis
BI biosynthesis
BL blood
CF cerebrospinal fluid
CH chemistry
CL classification
CS chemical synthesis
DE drug effects
EC economics
GE genetics
HI history
IM immunology
IP isolation & purification
ME metabolism
PD pharmacology
PH physiology
PK pharmacokinetics
PO poisoning
RE radiation effects
SD supply & distribution
ST standards
TO toxicity
TU therapeutic use
UL ultrastructure
UR urine
Entry Combination: deficiency:Leukokeratosis, Hereditary Mucosal
Previous Indexing: Keratins (1989-2006)
Public MeSH Note: 2007; for CYTOKERATIN-4 see KERATIN 1989-2006
History Note: 2007(1989)
DeCS ID: 52197
Unique ID: D053527
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2007/01/01
Date of Entry: 2006/07/05
Keratin-4 - Preferred
Concept UI M0011949
Scope note A type II keratin that is found associated with the KERATIN-13 in the internal stratified EPITHELIUM. Defects in gene for keratin-4 are a cause of HEREDITARY MUCOSAL LEUKOKERATOSIS.
Preferred term Keratin-4
Entry term(s) Cytokeratin 4
Cytokeratin-4
Keratin 4



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