MeSH Browser

MeSH Heading: Hypertelorism
Tree Number(s): C05.116.099.370.231.480; C05.660.207.231.480; C16.131.621.207.231.480
Unique ID: D006972
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D006972
Annotation: a form of craniofacial dysostosis; do not use /‌congen & do not coord with INFANT, NEWBORN, DISEASES
Scope Note: Abnormal increase in the interorbital distance due to overdevelopment of the lesser wings of the sphenoid.
NLM Classification #: WE 705
Public MeSH Note: 91; was see under BONE DISEASES, DEVELOPMENTAL 1985-90; was see under CRANIOFACIAL DYSOSTOSIS 1963-84
Online Note: search CRANIOFACIAL DYSOSTOSIS 1966-74
History Note: 91(75); was see under BONE DISEASES, DEVELOPMENTAL 1985-90; was see under CRANIOFACIAL DYSOSTOSIS 1963-84
Date Established: 1991/01/01
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)

Hypertelorism MeSH Descriptor Data 2024