Craniofacial Abnormalities [kraniofaciální abnormality]
Congenital structural deformities, malformations, or other abnormalities of the cranium and facial bones.
- Annotation
- general or unspecified; prefer specifics
- DUI
- D019465 MeSH Browser
- CUI
- M0028956
- Previous indexing
- Facial Bones (1966-1996); Skull/abnormalities (1966-1996)
- History note
- 97
- Public note
- 97
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 5
- CO
- complications 3
- DI
- diagnosis 19
- DG
- diagnostic imaging 4
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology 1
- EN
- enzymology
- EP
- epidemiology 3
- EH
- ethnology
- ET
- etiology 9
- GE
- genetics 15
- HI
- history 1
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 10
- PP
- physiopathology
- PC
- prevention & control
- PX
- psychology 1
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery 11
- TH
- therapy 8
- UR
- urine
- VE
- veterinary
- VI
- virology
3C syndrome Disease MeSH Browser
Abidi X-linked mental retardation syndrome Disease MeSH Browser
Alopecia, epilepsy, pyorrhea, mental subnormality Disease MeSH Browser
Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Disease MeSH Browser
Arthrogryposis multiplex congenita whistling face Disease MeSH Browser
Arthrogryposis, distal, with hypopituitarism, mental retardation, and facial anomalies Disease MeSH Browser
Arthrogryposis-like hand anomaly and sensorineural deafness Disease MeSH Browser
Arthropathy, Erosive Disease MeSH Browser
Asymmetric Short Stature Syndrome Disease MeSH Browser
B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations Disease MeSH Browser
Baker Vinters syndrome Disease MeSH Browser
Birk-Barel Mental Retardation Dysmorphism Syndrome Disease MeSH Browser
Blepharochalasis And Double Lip Disease MeSH Browser
Blepharophimosis with Facial and Genital Anomalies and Mental Retardation Disease MeSH Browser
Brachymesomelia renal syndrome Disease MeSH Browser
Brachyphalangy, polydactyly, and tibial aplasia-hypoplasia Disease MeSH Browser
Brachytelephalangy characteristic facies Kallmann Disease MeSH Browser
Branchial Cleft Anomalies Disease MeSH Browser
CODAS syndrome Disease MeSH Browser
Calvarial hyperostosis Disease MeSH Browser
Camptodactyly syndrome Guadalajara type 2 Disease MeSH Browser
Cerebrofrontofacial Syndrome Disease MeSH Browser
Cerebrooculofacioskeletal Syndrome 2 Disease MeSH Browser
Cerebrooculofacioskeletal Syndrome 4 Disease MeSH Browser
Cerebrooculonasal Syndrome Disease MeSH Browser
Chromosome 18 Pericentric Inversion Disease MeSH Browser
Chromosome 2p16.1-P15 Deletion Syndrome Disease MeSH Browser
Chromosome 2q31.2 Deletion Syndrome Disease MeSH Browser
Chromosome Xq28 Duplication Syndrome Disease MeSH Browser
Cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss Disease MeSH Browser
Combined Oxidative Phosphorylation Deficiency 2 Disease MeSH Browser
Congenital Cataracts, Facial Dysmorphism, And Neuropathy Disease MeSH Browser
Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence Disease MeSH Browser
Cortical Dysplasia-Focal Epilepsy Syndrome Disease MeSH Browser
Cranioacrofacial Syndrome Disease MeSH Browser
Craniodiaphyseal Dysplasia Disease MeSH Browser
Craniodiaphyseal Dysplasia, Autosomal Dominant Disease MeSH Browser
Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation Disease MeSH Browser
Craniofacial Anomalies, Empty Sella Turcica, Corneal Endothelial Changes, and Abnormal Retinal and Auditory Bipolar Cells Disease MeSH Browser
Craniofacial deafness hand syndrome Disease MeSH Browser
Craniofacial dyssynostosis Disease MeSH Browser
Craniofacioskeletal Syndrome Disease MeSH Browser
Craniofrontonasal dysplasia Disease MeSH Browser
Craniolenticulosutural Dysplasia Disease MeSH Browser
Craniomicromelic Syndrome Disease MeSH Browser
Craniorhiny Disease MeSH Browser
Curly hair-acral keratoderma-caries syndrome Disease MeSH Browser
Desbuquois syndrome Disease MeSH Browser
Diaphanospondylodysostosis Disease MeSH Browser
Digitorenocerebral Syndrome Disease MeSH Browser
Ectopia Lentis, Spontaneous Filtering Blebs, and Craniofacial Dysmorphism Disease MeSH Browser
Exchondrosis Of Pinna, Posterior Disease MeSH Browser
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis Disease MeSH Browser
Facial Dysmorphism with Multiple Malformations Disease MeSH Browser
Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly Disease MeSH Browser
Faciocardiomelic Syndrome Disease MeSH Browser
Fg Syndrome 5 Disease MeSH Browser
Floating-harbor syndrome Disease MeSH Browser
Forebrain Defects Disease MeSH Browser
Fountain syndrome Disease MeSH Browser
Fragile Site 16p12 Disease MeSH Browser
Fraser-Like Syndrome Disease MeSH Browser
Fronto-facio-nasal dysplasia Disease MeSH Browser
Frontonasal dysplasia Disease MeSH Browser
Frontoocular Syndrome Disease MeSH Browser
Frontootopalatodigital Osteodysplasia Disease MeSH Browser
Fryns-Aftimos Syndrome Disease MeSH Browser
Game Friedman Paradice syndrome Disease MeSH Browser
Genitopatellar Syndrome Disease MeSH Browser
Goldberg-Shprintzen megacolon syndrome Disease MeSH Browser
Gomez Lopez Hernandez syndrome Disease MeSH Browser
Gracile bone dysplasia Disease MeSH Browser
Grant syndrome Disease MeSH Browser
Hall Riggs mental retardation syndrome Disease MeSH Browser
Hanhart syndrome Disease MeSH Browser
Harrod Doman Keele syndrome Disease MeSH Browser
Haspeslagh Fryns Muelenaere syndrome Disease MeSH Browser
Hecht Scott syndrome Disease MeSH Browser
Hennekam lymphangiectasia lymphedema syndrome Disease MeSH Browser
Humeroradial Synostosis with Craniofacial Anomalies Disease MeSH Browser
Hypotonia-Cystinuria Syndrome Disease MeSH Browser
Ichthyosis cheek eyebrow syndrome Disease MeSH Browser
Jequier Kozlowski skeletal dysplasia Disease MeSH Browser
Jones Hersh Yusk syndrome Disease MeSH Browser
Kapur Toriello syndrome Disease MeSH Browser
Kleefstra Syndrome Disease MeSH Browser
Kosztolanyi syndrome Disease MeSH Browser
LIG4 Syndrome Disease MeSH Browser
Larsen syndrome, dominant type Disease MeSH Browser
Leichtman Wood Rohn syndrome Disease MeSH Browser
Lujan Fryns syndrome Disease MeSH Browser
Malpuech facial clefting syndrome Disease MeSH Browser
Mandibuloacral dysplasia with type B lipodystrophy Disease MeSH Browser
Mandibulofacial Dysostosis Syndrome, Bauru Type Disease MeSH Browser
Mandibulofacial Dysostosis with Macroblepharon and Macrostomia Disease MeSH Browser
Marshall syndrome Disease MeSH Browser
Marshall-Smith syndrome Disease MeSH Browser
Mental Retardation with Optic Atrophy, Facial Dysmorphism, Microcephaly, and Short Stature Disease MeSH Browser
Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism Disease MeSH Browser
Microcephaly, Facial Abnormalities, Micromelia, and Mental Retardation Disease MeSH Browser
Microphthalmia with Cyst, Bilateral Facial Clefts, and Limb Anomalies Disease MeSH Browser
Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia Disease MeSH Browser
Midline brainstem cleft Disease MeSH Browser
Morillo-Cucci Passarge syndrome Disease MeSH Browser
Myasthenic Syndrome, Congenital, with Facial Dysmorphism, associated with Acetylcholine Receptor Deficiency Disease MeSH Browser
Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay Disease MeSH Browser
NF1 Microdeletion Syndrome Disease MeSH Browser
Nablus mask-like facial syndrome Disease MeSH Browser
Neurofaciodigitorenal syndrome Disease MeSH Browser
Oculoauriculofrontonasal syndrome Disease MeSH Browser
Oculocerebral hypopigmentation syndrome type Preus Disease MeSH Browser
Oculodentodigital Dysplasia Disease MeSH Browser
Oculodentodigital Dysplasia, Autosomal Recessive Disease MeSH Browser
Oculootofacial Dysplasia Disease MeSH Browser
Orbital Margin, Hypoplasia of Disease MeSH Browser
Oto-Palato-digital syndrome type 1 Disease MeSH Browser
Oto-palato-digital syndrome, type 2 Disease MeSH Browser
Otocephaly Disease MeSH Browser
Otofacioosseous-Gonadal Syndrome Disease MeSH Browser
Otopalatodigital Spectrum Disorder Disease MeSH Browser
Pallister W syndrome Disease MeSH Browser
Pashayan syndrome Disease MeSH Browser
Pointer syndrome Disease MeSH Browser
Potato nose Disease MeSH Browser
Preauricular Fistulae, Congenital Disease MeSH Browser
Prieto X-linked mental retardation syndrome Disease MeSH Browser
Pseudoaminopterin syndrome Disease MeSH Browser
Reardon Hall Slaney syndrome Disease MeSH Browser
Riddle Syndrome Disease MeSH Browser
Roberts Syndrome Disease MeSH Browser
Robinow Syndrome Disease MeSH Browser
Rommen Mueller Sybert syndrome Disease MeSH Browser
Rozin Hertz Goodman syndrome Disease MeSH Browser
SCARF syndrome Disease MeSH Browser
Say Meyer syndrome Disease MeSH Browser
Schaefer Stein Oshman syndrome Disease MeSH Browser
Schilbach-Rott Syndrome Ocular Hypotelorism, Submucosal Cleft Palate, and Hypospadias Disease MeSH Browser
Schinzel-Giedion syndrome Disease MeSH Browser
Schwartz-Lelek syndrome Disease MeSH Browser
Scimitar Anomaly, Multiple Cardiac Malformations, and Craniofacial and Central Nervous System Abnormalities Disease MeSH Browser
Seaver Cassidy syndrome Disease MeSH Browser
Seckel like syndrome type Buebel Disease MeSH Browser
Sener syndrome Disease MeSH Browser
Short Stature And Facioauriculothoracic Malformations Disease MeSH Browser
Short Stature-Obesity Syndrome Disease MeSH Browser
Simosa cranio facial syndrome Disease MeSH Browser
Sonoda syndrome Disease MeSH Browser
Splenogonadal fusion limb defects micrognatia Disease MeSH Browser
Spondyloepimetaphyseal Dysplasia, Aggrecan Type Disease MeSH Browser
Spondyloocular Syndrome, Autosomal Recessive Disease MeSH Browser
Stickler Syndrome, Autosomal Recessive, COL9A1-Related Disease MeSH Browser
Teebi Shaltout syndrome Disease MeSH Browser
Telecanthus Disease MeSH Browser
Temtamy syndrome Disease MeSH Browser
Ter Haar syndrome Disease MeSH Browser
Tetrasomy X Disease MeSH Browser
Tollner Horst Manzke syndrome Disease MeSH Browser
Tricho-dento-osseous syndrome Disease MeSH Browser
Urioste Martinez-Frias syndrome Disease MeSH Browser
Van Bogaert-Hozay syndrome Disease MeSH Browser
Van Buchem disease type 2 Disease MeSH Browser
Van Maldergem Wetzburger Verloes syndrome Disease MeSH Browser
Vertebral body fusion overgrowth Disease MeSH Browser
Viljoen Kallis Voges syndrome Disease MeSH Browser
Weaver syndrome Disease MeSH Browser
Weaver-Like Syndrome Disease MeSH Browser
Wiedemann Grosse Dibbern syndrome Disease MeSH Browser
Winter Shortland Temple syndrome Disease MeSH Browser
Zimmerman Laband syndrome Disease MeSH Browser
Narrower terms
- 22q11 Deletion Syndrome
- Cleidocranial Dysplasia
- Costello Syndrome
- Craniofacial Dysostosis
- Craniosynostoses
- Donohue Syndrome
- Holoprosencephaly
- LEOPARD Syndrome
- Loeys-Dietz Syndrome
- Maxillofacial Abnormalities
- Megalencephaly
- Microcephaly
- Noonan Syndrome
- Orofaciodigital Syndromes
- Plagiocephaly
- Platybasia
- Rubinstein-Taybi Syndrome
- Silver-Russell Syndrome