MeSH Browser

MeSH Heading: Basal Cell Nevus Syndrome
Tree Number(s): C04.182.089.530.690.150; C04.557.470.200.165.150; C04.557.470.565.165.150; C04.700.175; C05.116.099.105; C05.500.470.690.150; C07.320.450.670.130; C16.131.077.130; C16.320.700.175
Unique ID: D001478
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D001478
Annotation: coordinate IM with precoordinated organ/neoplasm (IM or NIM) only if pertinent; do not confuse entry term GORLIN-GOLTZ SYNDROME with GOLTZ- GORLIN SYNDROME see FOCAL DERMAL HYPOPLASIA
Scope Note: Hereditary disorder consisting of multiple basal cell carcinomas, odontogenic keratocysts, and multiple skeletal defects, e.g., frontal and temporoparietal bossing, bifurcated and splayed ribs, kyphoscoliosis, fusion of vertebrae, and cervicothoracic spina bifida. Genetic transmission is autosomal dominant.
Entry Term(s): Fifth Phacomatosis; Gorlin Syndrome; Gorlin-Goltz Syndrome; Multiple Basal Cell Nevi, Odontogenic Keratocysts, and Skeletal Anomalies; NBCCS; Nevoid Basal Cell Carcinoma Syndrome; Nevus Syndrome, Basal Cell
Previous Indexing: Bone Cyst (1966-1979); Carcinoma, Basal Cell (1966-1979); Jaw Diseases (1967-1979); Jaw Neoplasms (1967-1979); Skin Neoplasms (1967-1979); Syndrome (1972-1979); specific jaw disease (1967-1979); specific jaw neoplasm (1967-1979)
Public MeSH Note: 91; was see under CARCINOMA, BASAL CELL 1980-90
History Note: 91(80); was see under CARCINOMA, BASAL CELL 1980-90
Date Established: 1991/01/01
Date of Entry: 1979/04/25
Revision Date: 2013/07/08

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)

Neoplasms [C04]
- Cysts [C04.182]
  - Bone Cysts [C04.182.089]
    - Jaw Cysts [C04.182.089.530]
      - Odontogenic Cysts [C04.182.089.530.690]
        
        Basal Cell Nevus Syndrome [C04.182.089.530.690.150]
        
        Dentigerous Cyst [C04.182.089.530.690.310]
        
        Odontogenic Cyst, Calcifying [C04.182.089.530.690.605]
        
        Periodontal Cyst [C04.182.089.530.690.790]

Neoplasms [C04]
- Neoplasms by Histologic Type [C04.557]
  - Neoplasms, Glandular and Epithelial [C04.557.470]
    - Carcinoma [C04.557.470.200]
      - Carcinoma, Basal Cell [C04.557.470.200.165]
        
        Basal Cell Nevus Syndrome [C04.557.470.200.165.150]

Neoplasms [C04]
- Neoplasms by Histologic Type [C04.557]
  - Neoplasms, Glandular and Epithelial [C04.557.470]
    - Neoplasms, Basal Cell [C04.557.470.565]
      - Carcinoma, Basal Cell [C04.557.470.565.165]
        
        Basal Cell Nevus Syndrome [C04.557.470.565.165.150]

Neoplasms [C04]
- Neoplastic Syndromes, Hereditary [C04.700]

Musculoskeletal Diseases [C05]
- Bone Diseases [C05.116]
  - Bone Diseases, Developmental [C05.116.099]

Musculoskeletal Diseases [C05]
- Jaw Diseases [C05.500]
  - Jaw Cysts [C05.500.470]
    - Odontogenic Cysts [C05.500.470.690]

Stomatognathic Diseases [C07]
- Jaw Diseases [C07.320]
  - Jaw Cysts [C07.320.450]
    - Odontogenic Cysts [C07.320.450.670]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Congenital Abnormalities [C16.131]
  - Abnormalities, Multiple [C16.131.077]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
  - Neoplastic Syndromes, Hereditary [C16.320.700]

Basal Cell Nevus Syndrome Preferred

Concept UI: M0002195
Scope Note: Hereditary disorder consisting of multiple basal cell carcinomas, odontogenic keratocysts, and multiple skeletal defects, e.g., frontal and temporoparietal bossing, bifurcated and splayed ribs, kyphoscoliosis, fusion of vertebrae, and cervicothoracic spina bifida. Genetic transmission is autosomal dominant.
Terms: Basal Cell Nevus Syndrome Preferred Term
Term UI T004294
Date01/01/1999
LexicalTag NON
ThesaurusID; Gorlin Syndrome
Term UI T004295
Date04/25/1979
LexicalTag EPO
ThesaurusID; Gorlin-Goltz Syndrome
Term UI T746381
Date02/24/2009
LexicalTag EPO
ThesaurusID; NBCCS
Term UI T843436
Date05/01/2013
LexicalTag NON
ThesaurusID; Nevoid Basal Cell Carcinoma Syndrome
Term UI T004296
Date04/25/1979
LexicalTag NON
ThesaurusID; Nevus Syndrome, Basal Cell
Term UI T004293
Date04/18/1986
LexicalTag NON
ThesaurusID UNK (19XX); Fifth Phacomatosis
Term UI T746383
Date02/24/2009
LexicalTag NON
ThesaurusID; Multiple Basal Cell Nevi, Odontogenic Keratocysts, and Skeletal Anomalies
Term UI T782123
Date12/14/2010
LexicalTag NON
ThesaurusID

Basal Cell Nevus Syndrome MeSH Descriptor Data 2024