Cleft Palate MeSH Descriptor Data 2024

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]

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]

Stomatognathic Diseases [C07]
- Mouth Diseases [C07.465]
  - Mouth Abnormalities [C07.465.525]

Stomatognathic Diseases [C07]
- Stomatognathic System Abnormalities [C07.650]
  - Maxillofacial Abnormalities [C07.650.500]
    - Jaw Abnormalities [C07.650.500.460]

Stomatognathic Diseases [C07]
- Stomatognathic System Abnormalities [C07.650]
  - Mouth Abnormalities [C07.650.525]

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 Palate Preferred

Cleft Palate, Isolated Narrower

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