Facies [faciální stigmatizace]

topical
31
Persistent link   https://www.medvik.cz/link/D019066
Definition

The appearance of the face that is often characteristic of a disease or pathological condition, as the elfin facies of WILLIAMS SYNDROME or facies of DOWN SYNDROME. (Random House Unabridged Dictionary, 2d ed)

Annotation
do not confuse with FACIAL EXPRESSION, a psychol response; coord IM with assoc dis (IM)
DUI
D019066 MeSH Browser
CUI
M0028463
History note
96; was see under FACIAL EXPRESSION 1963-73
Online note
use FACIAL EXPRESSION to search FACIES 1966-73
Public note
96; was see under FACIAL EXPRESSION 1963-73

C Diseases
C23.550.291 Disease Attributes 1 208
C23.550.291.125 Acute Disease 2 707
C23.550.291.187 Asymptomatic Diseases 109
C23.550.291.219 Breakthrough Infections 1
C23.550.291.250 Catastrophic Illness 23
C23.550.291.500 Chronic Disease 5 060
C23.550.291.531 Communicable Diseases 3 450
C23.550.291.562 Convalescence 118
C23.550.291.625 Critical Illness 738
C23.550.291.656 Disease Progression 3 149
C23.550.291.671 Disease Resistance 72
C23.550.291.687 Disease Susceptibility 289
C23.550.291.750 Diseases in Twins 86
C23.550.291.781 Emergencies 1 066
C23.550.291.812 Facies 31
C23.550.291.875 Iatrogenic Disease 617
C23.550.291.883 Late Onset Disorders 8
C23.550.291.890 Neglected Diseases 18
C23.550.291.898 Noncommunicable Diseases 34
C23.550.291.902 Persistent Infection 8
C23.550.291.906 Rare Diseases 756
C23.550.291.937 Recurrence 3 222
C23.550.291.968 Undiagnosed Diseases 4

E Analytical, Diagnostic and Therapeutic Techniques and Equipment
E01 Diagnosis 1 793
E01.370.600 Physical Examination 659
E01.370.600.024 Anthropometry 1 682
E01.370.600.050 Apgar Score 84
E01.370.600.060 Auscultation 79
E01.370.600.100 Blood Pressure Determination 1 487
E01.370.600.115 Body Constitution 195
E01.370.600.225 Facial Expression 116
E01.370.600.230 Facies 31
E01.370.600.250 Gait 442
E01.370.600.293 Gynecological Examination 83
E01.370.600.315 Heart Rate Determination 27
E01.370.600.337 Metabolic Equivalent 8
E01.370.600.425 Muscle Strength 393
E01.370.600.550 Neurologic Examination 610
E01.370.600.600 Palpation 163
E01.370.600.610 Percussion 45
E01.370.600.620 Pigmentation 145
E01.370.600.700 Range of Motion, Articular 434
E01.370.600.750 Self-Examination 62
E01.370.600.875 Vital Signs 15

Al Gazali Aziz Salem syndrome Disease MeSH Browser

Al Gazali Hirschsprung syndrome Disease MeSH Browser

Anonychia-onychodystrophy with hypoplasia or absence of distal phalanges Disease MeSH Browser

Aortic arch anomaly with peculiar facies and mental retardation Disease MeSH Browser

Arthrogryposis, Distal, with Mental Retardation and Characteristic Facies Disease MeSH Browser

Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities Disease MeSH Browser

Bainbridge-Ropers syndrome Chemical MeSH Browser

Beemer Ertbruggen syndrome Disease MeSH Browser

Boomerang dysplasia Disease MeSH Browser

Bowen syndrome Disease MeSH Browser

Brachytelephalangy characteristic facies Kallmann Disease MeSH Browser

Brunoni syndrome Disease MeSH Browser

Burn-Mckeown syndrome Disease MeSH Browser

Cardiofaciocutaneous syndrome Disease MeSH Browser

Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stature, and Mental Retardation Disease MeSH Browser

Charcot-Marie-Tooth Disease, Guadalajara Neuronal Type Disease MeSH Browser

Chondrodysplasia, Megarbane-Dagher-Melki Type Disease MeSH Browser

Chromosome 10q26 Deletion Syndrome Disease MeSH Browser

Chromosome 5p13 Duplication Syndrome Disease MeSH Browser

Chromosome Xq28 Duplication Syndrome Disease MeSH Browser

Clark-Baraitser syndrome Disease MeSH Browser

Cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss Disease MeSH Browser

Coarse facial features Disease MeSH Browser

Cortical Blindness, Retardation, and Postaxial Polydactyly Disease MeSH Browser

Craniosynostosis, Calcification of Basal Ganglia, and Facial Dysmorphism Disease MeSH Browser

Creases, Infra-Auricular Cutaneous, with Tall Stature and Advanced Bone Age Disease MeSH Browser

Cree Mental Retardation Syndrome Disease MeSH Browser

Crisponi syndrome Disease MeSH Browser

Crumpled helices and small mouth Disease MeSH Browser

Cubitus Valgus with Mental Retardation and Unusual Facies Disease MeSH Browser

Cyprus facial neuromusculoskeletal syndrome Disease MeSH Browser

Davis Lafer syndrome Disease MeSH Browser

Deafness-Craniofacial Syndrome Disease MeSH Browser

Der Kaloustian Mcintosh Silver syndrome Disease MeSH Browser

Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis Disease MeSH Browser

Dislocation of Hip, Congenital, with Hyperextensibility of Fingers and Facial Dysmorphism Disease MeSH Browser

Disproportionate Short Stature with Ptosis and Valvular Heart Lesions Disease MeSH Browser

Dubowitz syndrome Disease MeSH Browser

Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet Disease MeSH Browser

Ectodermal dysplasia alopecia preaxial polydactyly Disease MeSH Browser

Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features Disease MeSH Browser

Ectrodactyly cardiopathy dysmorphism Disease MeSH Browser

Edinburgh Malformation Syndrome Disease MeSH Browser

FACES syndrome Disease MeSH Browser

Facial Dysmorphism, Selective Tooth Agenesis, and Choroid Calcification Disease MeSH Browser

Faciocardiomelic Syndrome Disease MeSH Browser

Feingold Trainer syndrome Disease MeSH Browser

Fibrochondrogenesis Disease MeSH Browser

Fibromatosis, Gingival, with Distinctive Facies Disease MeSH Browser

Filippi syndrome Disease MeSH Browser

Fryns Macrocephaly Disease MeSH Browser

Fryns syndrome Disease MeSH Browser

Fryns-Aftimos Syndrome Disease MeSH Browser

Giacheti Syndrome Disease MeSH Browser

Granddad Syndrome Disease MeSH Browser

Growth Deficiency and Mental Retardation with Facial Dysmorphism Disease MeSH Browser

Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Disease MeSH Browser

Growth mental deficiency syndrome of Myhre Disease MeSH Browser

Hadziselimovic Syndrome Disease MeSH Browser

Haspeslagh Fryns Muelenaere syndrome Disease MeSH Browser

Helsmoortel-Van der Aa syndrome Chemical MeSH Browser

Holoprosencephaly 10 Disease MeSH Browser

Hydronephrosis, Congenital, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardation Disease MeSH Browser

Hydrops Fetalis, Nonimmune, With Gracile Bones And Dysmorphic Features Disease MeSH Browser

Hypotonia, Seizures, And Precocious Puberty Disease MeSH Browser

Iris dysplasia hypertelorism deafness Disease MeSH Browser

Irons Bhan syndrome Disease MeSH Browser

KBG syndrome Disease MeSH Browser

Kahrizi Syndrome Disease MeSH Browser

Kaufman oculocerebrofacial syndrome Disease MeSH Browser

Kozlowski Rafinski Klicharska syndrome Disease MeSH Browser

Kozlowski-Krajewska syndrome Disease MeSH Browser

Larsen-Like Syndrome Disease MeSH Browser

Leri pleonosteosis Disease MeSH Browser

Lichtenstein syndrome Disease MeSH Browser

Lymphedema, Cardiac Septal Defects, And Characteristic Facies Disease MeSH Browser

Lymphedema, microcephaly and chorioretinopathy syndrome Disease MeSH Browser

Macrocephaly Autism Syndrome Disease MeSH Browser

Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies Disease MeSH Browser

Malocclusion and Short Stature Disease MeSH Browser

Marfanoid Mental Retardation Syndrome, Autosomal Disease MeSH Browser

McDonough syndrome Disease MeSH Browser

McPherson Clemens syndrome Disease MeSH Browser

Mental Retardation, Buenos Aires Type Disease MeSH Browser

Mental Retardation, Microcephaly, Epilepsy, And Coarse Face Disease MeSH Browser

Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations Disease MeSH Browser

Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly Disease MeSH Browser

Microcephaly cervical spine fusion anomalies Disease MeSH Browser

Microcephaly deafness syndrome Disease MeSH Browser

Microcephaly with Chemotactic Defect and Transient Hypogammaglobulinemia Disease MeSH Browser

Microcephaly, Growth Retardation, Cataract, Hearing Loss, And Unusual Appearance Disease MeSH Browser

Microcephaly, Severe, with Skeletal Anomalies including Posterior Rib-Gap Defects Disease MeSH Browser

Micromelic dysplasia, congenital, with dislocation of radius Disease MeSH Browser

Mowat-Wilson syndrome Disease MeSH Browser

Multiple Pterygium Syndrome, X-Linked Disease MeSH Browser

NF1 Microduplication Syndrome Disease MeSH Browser

Nicolaides Baraitser syndrome Disease MeSH Browser

Night blindness skeletal anomalies unusual facies Disease MeSH Browser

O'Donnell-Luria-Rodan syndrome Disease MeSH Browser

Omodysplasia 2 Disease MeSH Browser

Oroacral Syndrome, Verloes-Koulischer Type Disease MeSH Browser

Osteolysis syndrome recessive Disease MeSH Browser

Otoonychoperoneal Syndrome Disease MeSH Browser

Palant cleft palate syndrome Disease MeSH Browser

Partington Anderson syndrome Disease MeSH Browser

Pfeiffer Palm Teller syndrome Disease MeSH Browser

Pierre Robin Sequence with Facial and Digital Anomalies Disease MeSH Browser

Pitt-Hopkins syndrome Disease MeSH Browser

Pituitary Hormone Deficiency, Combined, 1 Disease MeSH Browser

Plantar Lipomatosis, Unusual Facies, and Developmental Delay Disease MeSH Browser

Progeroid Facial Appearance with Hand Anomalies Disease MeSH Browser

Radioulnar synostosis retinal pigment abnormalities Disease MeSH Browser

Ramos Arroyo Clark syndrome Disease MeSH Browser

Renal Tubular Acidosis, Distal, With Nephrocalcinosis, Short Stature, Mental Retardation, And Distinctive Facies Disease MeSH Browser

Renal and Mullerian Duct Hypoplasia Disease MeSH Browser

Renal dysplasia - limb defects syndrome Disease MeSH Browser

Robin Sequence with Distinctive Facial Appearance and Brachydactyly Disease MeSH Browser

Roifman-Chitayat Syndrome Disease MeSH Browser

Rudiger Syndrome Disease MeSH Browser

Ruvalcaba Syndrome Disease MeSH Browser

Schaaf-Yang syndrome Chemical MeSH Browser

Schrander-Stumpel Theunissen Hulsmans syndrome Disease MeSH Browser

Seckel Syndrome 3 Disease MeSH Browser

Seckel syndrome 1 Disease MeSH Browser

Short Stature, Facial Dysmorphism, Severe Brachydactyly, and Syndactyly Disease MeSH Browser

Shprintzen omphalocele syndrome Disease MeSH Browser

Snijders Blok-Campeau syndrome Disease MeSH Browser

Spastic paraplegia 23 Disease MeSH Browser

Speech Development, Delayed, With Facial Asymmetry, Strabismus, And Transverse Earlobe Crease Disease MeSH Browser

Spinocerebellar Ataxia with Dysmorphism Disease MeSH Browser

Spondyloepiphyseal Dysplasia Tarda with Characteristic Facies Disease MeSH Browser

Temple syndrome Disease MeSH Browser

Thakker Donnai syndrome Disease MeSH Browser

Thomas Jewett Raines syndrome Disease MeSH Browser

Thrombocytopenia Robin sequence Disease MeSH Browser

Trichohepatoenteric Syndrome Disease MeSH Browser

Trichorhinophalangeal Syndrome, Type III Disease MeSH Browser

Urofacial syndrome Disease MeSH Browser

Uruguay Faciocardiomusculoskeletal Syndrome Disease MeSH Browser

White forelock with malformations Disease MeSH Browser

Winter Harding Hyde syndrome Disease MeSH Browser

Young Simpson syndrome Disease MeSH Browser

Zechi-Ceide Syndrome Disease MeSH Browser