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Craniofacial Abnormalities
MeSH Descriptor Data 2025
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Craniofacial Abnormalities
Tree Number(s)
C05.660.207
C16.131.621.207
Unique ID
D019465
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D019465
Annotation
general or unspecified; prefer specifics
Scope Note
Congenital structural deformities, malformations, or other abnormalities of the cranium and facial bones.
Entry Version
CRANIOFACIAL ABNORM
NLM Classification #
WE 705
Previous Indexing
Facial Bones (1966-1996)
Skull/abnormalities (1966-1996)
Public MeSH Note
97
History Note
97
Date Established
1997/01/01
Date of Entry
1996/06/10
Revision Date
1999/11/03
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]
Musculoskeletal Abnormalities [C05.660]
Arthrogryposis [C05.660.077]
Campomelic Dysplasia [C05.660.142]
Craniofacial Abnormalities [C05.660.207]
22q11 Deletion Syndrome [C05.660.207.103]
Cleidocranial Dysplasia [C05.660.207.207]
Costello Syndrome [C05.660.207.219]
Craniofacial Dysostosis [C05.660.207.231]
Craniosynostoses [C05.660.207.240]
Donohue Syndrome [C05.660.207.325]
Holoprosencephaly [C05.660.207.410]
LEOPARD Syndrome [C05.660.207.525]
Loeys-Dietz Syndrome [C05.660.207.532]
Megalencephaly [C05.660.207.536]
Maxillofacial Abnormalities [C05.660.207.540]
Microcephaly [C05.660.207.620]
Noonan Syndrome [C05.660.207.690]
Orofaciodigital Syndromes [C05.660.207.700]
Plagiocephaly [C05.660.207.707]
Platybasia [C05.660.207.720]
Rubinstein-Taybi Syndrome [C05.660.207.850]
Silver-Russell Syndrome [C05.660.207.925]
Developmental Dysplasia of the Hip [C05.660.297]
Funnel Chest [C05.660.386]
Gastroschisis [C05.660.417]
Klippel-Feil Syndrome [C05.660.551]
Limb Deformities, Congenital [C05.660.585]
Pectus Carinatum [C05.660.745]
Synostosis [C05.660.906]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Musculoskeletal Abnormalities [C16.131.621]
Arthrogryposis [C16.131.621.077]
Campomelic Dysplasia [C16.131.621.142]
Cervical Rib Syndrome [C16.131.621.174]
Craniofacial Abnormalities [C16.131.621.207]
22q11 Deletion Syndrome [C16.131.621.207.103]
Cleidocranial Dysplasia [C16.131.621.207.207]
Craniofacial Dysostosis [C16.131.621.207.231]
Craniosynostoses [C16.131.621.207.240]
Holoprosencephaly [C16.131.621.207.410]
LEOPARD Syndrome [C16.131.621.207.525]
Megalencephaly [C16.131.621.207.532]
Maxillofacial Abnormalities [C16.131.621.207.540]
Microcephaly [C16.131.621.207.620]
Noonan Syndrome [C16.131.621.207.690]
Orofaciodigital Syndromes [C16.131.621.207.700]
Plagiocephaly [C16.131.621.207.707]
Platybasia [C16.131.621.207.720]
Rubinstein-Taybi Syndrome [C16.131.621.207.850]
Developmental Dysplasia of the Hip [C16.131.621.297]
Funnel Chest [C16.131.621.386]
Gastroschisis [C16.131.621.417]
Hajdu-Cheney Syndrome [C16.131.621.445]
Hip Dislocation, Congenital [C16.131.621.449]
Klippel-Feil Syndrome [C16.131.621.551]
Laryngomalacia [C16.131.621.568]
Limb Deformities, Congenital [C16.131.621.585]
Pectus Carinatum [C16.131.621.745]
Synostosis [C16.131.621.906]
Tracheobronchomalacia [C16.131.621.953]
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Craniofacial Abnormalities
Preferred
Concept UI
M0028956
Scope Note
Congenital structural deformities, malformations, or other abnormalities of the cranium and facial bones.
Terms
Craniofacial Abnormalities
Preferred Term
Term UI
T058021
Date
01/01/1999
LexicalTag
NON
ThesaurusID
NLM (1997)
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