Toggle navigation
Search
Tree View
MeSH on Demand
MeSH 2024
About
Suggestions
Contact Us
Cleft Palate
MeSH Descriptor Data 2025
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Cleft Palate
Tree Number(s)
C05.500.460.185
C05.660.207.540.460.185
C07.320.440.185
C07.465.525.185
C07.650.500.460.185
C07.650.525.185
C16.131.621.207.540.460.185
C16.131.850.500.460.185
C16.131.850.525.185
Unique ID
D002972
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D002972
Annotation
do not use
/congen
& do not coord with
INFANT, NEWBORN, DISEASES
; when with
CLEFT LIP
, do not also use
ABNORMALITIES, MULTIPLE
Scope Note
Congenital fissure of the soft and/or hard palate, due to faulty fusion.
Entry Term(s)
Cleft Palate, Isolated
NLM Classification #
WV 440
Date Established
1966/01/01
Date of Entry
1999/01/01
Revision Date
2012/07/03
Allowable Qualifiers
blood (BL)
cerebrospinal fluid (CF)
chemically induced (CI)
classification (CL)
complications (CO)
diagnosis (DI)
diagnostic imaging (DG)
diet therapy (DH)
drug therapy (DT)
economics (EC)
embryology (EM)
enzymology (EN)
epidemiology (EP)
ethnology (EH)
etiology (ET)
genetics (GE)
history (HI)
immunology (IM)
metabolism (ME)
microbiology (MI)
mortality (MO)
nursing (NU)
parasitology (PS)
pathology (PA)
physiopathology (PP)
prevention & control (PC)
psychology (PX)
radiotherapy (RT)
rehabilitation (RH)
surgery (SU)
therapy (TH)
urine (UR)
veterinary (VE)
virology (VI)
Musculoskeletal Diseases [C05]
Jaw Diseases [C05.500]
Jaw Abnormalities [C05.500.460]
Cleft Palate [C05.500.460.185]
Micrognathism [C05.500.460.457]
Pierre Robin Syndrome [C05.500.460.606]
Prognathism [C05.500.460.655]
Retrognathia [C05.500.460.827]
Musculoskeletal Diseases [C05]
Musculoskeletal Abnormalities [C05.660]
Craniofacial Abnormalities [C05.660.207]
Maxillofacial Abnormalities [C05.660.207.540]
Jaw Abnormalities [C05.660.207.540.460]
Cleft Palate [C05.660.207.540.460.185]
Micrognathism [C05.660.207.540.460.457]
Pierre Robin Syndrome [C05.660.207.540.460.606]
Prognathism [C05.660.207.540.460.655]
Retrognathia [C05.660.207.540.460.827]
Stomatognathic Diseases [C07]
Jaw Diseases [C07.320]
Jaw Abnormalities [C07.320.440]
Cleft Palate [C07.320.440.185]
Micrognathism [C07.320.440.457]
Pierre Robin Syndrome [C07.320.440.606]
Prognathism [C07.320.440.655]
Retrognathia [C07.320.440.827]
Stomatognathic Diseases [C07]
Mouth Diseases [C07.465]
Mouth Abnormalities [C07.465.525]
Cleft Lip [C07.465.525.164]
Cleft Palate [C07.465.525.185]
Fibromatosis, Gingival [C07.465.525.304]
Macrostomia [C07.465.525.480]
Microstomia [C07.465.525.520]
Velopharyngeal Insufficiency [C07.465.525.955]
Stomatognathic Diseases [C07]
Stomatognathic System Abnormalities [C07.650]
Maxillofacial Abnormalities [C07.650.500]
Jaw Abnormalities [C07.650.500.460]
Cleft Palate [C07.650.500.460.185]
Micrognathism [C07.650.500.460.457]
Pierre Robin Syndrome [C07.650.500.460.606]
Prognathism [C07.650.500.460.655]
Retrognathia [C07.650.500.460.827]
Stomatognathic Diseases [C07]
Stomatognathic System Abnormalities [C07.650]
Mouth Abnormalities [C07.650.525]
Cleft Lip [C07.650.525.164]
Cleft Palate [C07.650.525.185]
Fibromatosis, Gingival [C07.650.525.304]
Macrostomia [C07.650.525.480]
Microstomia [C07.650.525.520]
Velopharyngeal Insufficiency [C07.650.525.955]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Musculoskeletal Abnormalities [C16.131.621]
Craniofacial Abnormalities [C16.131.621.207]
Maxillofacial Abnormalities [C16.131.621.207.540]
Jaw Abnormalities [C16.131.621.207.540.460]
Cleft Palate [C16.131.621.207.540.460.185]
Micrognathism [C16.131.621.207.540.460.457]
Pierre Robin Syndrome [C16.131.621.207.540.460.606]
Prognathism [C16.131.621.207.540.460.655]
Retrognathia [C16.131.621.207.540.460.827]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Stomatognathic System Abnormalities [C16.131.850]
Maxillofacial Abnormalities [C16.131.850.500]
Jaw Abnormalities [C16.131.850.500.460]
Cleft Palate [C16.131.850.500.460.185]
Micrognathism [C16.131.850.500.460.457]
Pierre Robin Syndrome [C16.131.850.500.460.606]
Prognathism [C16.131.850.500.460.655]
Retrognathia [C16.131.850.500.460.827]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Stomatognathic System Abnormalities [C16.131.850]
Mouth Abnormalities [C16.131.850.525]
Cleft Lip [C16.131.850.525.164]
Cleft Palate [C16.131.850.525.185]
Fibromatosis, Gingival [C16.131.850.525.304]
Macrostomia [C16.131.850.525.480]
Microstomia [C16.131.850.525.520]
Velopharyngeal Insufficiency [C16.131.850.525.955]
Expand All
Collapse All
Cleft Palate
Preferred
Concept UI
M0004549
Scope Note
Congenital fissure of the soft and/or hard palate, due to faulty fusion.
Terms
Cleft Palate
Preferred Term
Term UI
T008588
Date
01/01/1999
LexicalTag
NON
ThesaurusID
Cleft Palate, Isolated
Narrower
Concept UI
M0574709
Terms
Cleft Palate, Isolated
Preferred Term
Term UI
T811464
Date
11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
page delivered in 0.187s