MeSH Browser

MeSH Heading: Branchio-Oto-Renal Syndrome
Tree Number(s): C16.131.077.208; C16.131.260.090; C16.320.180.090
Unique ID: D019280
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D019280
Scope Note: An autosomal dominant disorder manifested by various combinations of preauricular pits, branchial fistulae or cysts, lacrimal duct stenosis, hearing loss, structural defects of the outer, middle, or inner ear, and renal dysplasia. Associated defects include asthenic habitus, long narrow facies, constricted palate, deep overbite, and myopia. Hearing loss may be due to Mondini type cochlear defect and stapes fixation. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed)
Entry Term(s): BOF Syndrome; BOR Syndrome; Branchial Clefts with Characteristic Facies, Growth Retardation, Imperforate Nasolacrimal Duct, and Premature Aging; Branchio-Oculo-Facial Syndrome; Branchio-Otorenal Dysplasia; Branchio-Otorenal Syndrome; Branchiooculofacial Syndrome; Branchiootorenal Dysplasia; Branchiootorenal Syndrome 1; Branchiootorenal Syndrome 2; Hemangiomatous Branchial Clefts-Lip Pseudocleft Syndrome; Lee Root Fenske Syndrome; Lip Pseudocleft-Hemangiomatous Branchial Cyst Syndrome; Melnick-Fraser Syndrome
Previous Indexing: Abnormalities, Multiple (1966-1996); Chromosome Abnormalities (1966-1996)
Public MeSH Note: 97
History Note: 97
Date Established: 1997/01/01
Date of Entry: 1996/06/10
Revision Date: 2019/05/17

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)

Concept UI: M0028709
Scope Note: An autosomal dominant disorder manifested by various combinations of preauricular pits, branchial fistulae or cysts, lacrimal duct stenosis, hearing loss, structural defects of the outer, middle, or inner ear, and renal dysplasia. Associated defects include asthenic habitus, long narrow facies, constricted palate, deep overbite, and myopia. Hearing loss may be due to Mondini type cochlear defect and stapes fixation. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed)
Terms: Branchio-Oto-Renal Syndrome Preferred Term
Term UI T057442
Date01/01/1999
LexicalTag NON
ThesaurusID; BOR Syndrome
Term UI T057441
Date11/29/1995
LexicalTag NON
ThesaurusID; Branchio-Otorenal Dysplasia
Term UI T057443
Date11/29/1995
LexicalTag NON
ThesaurusID; Branchio-Otorenal Syndrome
Term UI T057444
Date11/29/1995
LexicalTag NON
ThesaurusID; Branchiootorenal Dysplasia
Term UI T845616
Date06/13/2013
LexicalTag NON
ThesaurusID; Melnick-Fraser Syndrome
Term UI T845620
Date06/13/2013
LexicalTag NON
ThesaurusID

Branchio-Oto-Renal Syndrome MeSH Descriptor Data 2025