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Hypertelorism
MeSH Descriptor Data 2024
Details
Qualifiers
MeSH Tree Structures
Concepts
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)
Musculoskeletal Diseases [C05]
Bone Diseases [C05.116]
Bone Diseases, Developmental [C05.116.099]
Dysostoses [C05.116.099.370]
Craniofacial Dysostosis [C05.116.099.370.231]
Hallermann's Syndrome [C05.116.099.370.231.427]
Hypertelorism [C05.116.099.370.231.480]
Mandibulofacial Dysostosis [C05.116.099.370.231.576]
Musculoskeletal Diseases [C05]
Musculoskeletal Abnormalities [C05.660]
Craniofacial Abnormalities [C05.660.207]
Craniofacial Dysostosis [C05.660.207.231]
Hallermann's Syndrome [C05.660.207.231.427]
Hypertelorism [C05.660.207.231.480]
Mandibulofacial Dysostosis [C05.660.207.231.576]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Musculoskeletal Abnormalities [C16.131.621]
Craniofacial Abnormalities [C16.131.621.207]
Craniofacial Dysostosis [C16.131.621.207.231]
Hallermann's Syndrome [C16.131.621.207.231.427]
Hypertelorism [C16.131.621.207.231.480]
Mandibulofacial Dysostosis [C16.131.621.207.231.576]
Expand All
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Hypertelorism
Preferred
Concept UI
M0010858
Scope Note
Abnormal increase in the interorbital distance due to overdevelopment of the lesser wings of the sphenoid.
Terms
Hypertelorism
Preferred Term
Term UI
T020936
Date
01/01/1999
LexicalTag
NON
ThesaurusID
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