serw-MX  [xml]  
 


    
 DeCS Categories

C05 Musculoskeletal Diseases .
C05.116 Bone Diseases .
C05.116.099 Bone Diseases, Developmental .
C05.116.099.370 Dysostoses .
C05.116.099.370.231 Craniofacial Dysostosis .
C05.116.099.370.231.576 Mandibulofacial Dysostosis .
C05.116.099.708 Osteochondrodysplasias .
C05.116.099.708.207 Cleidocranial Dysplasia .
C05.660 Musculoskeletal Abnormalities .
C05.660.207 Craniofacial Abnormalities .
C05.660.207.207 Cleidocranial Dysplasia .
C05.660.207.231 Craniofacial Dysostosis .
C05.660.207.231.576 Mandibulofacial Dysostosis .
C10 Nervous System Diseases .
C10.597 Neurologic Manifestations .
C10.597.751 Sensation Disorders .
C10.597.751.600 Olfaction Disorders .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.621 Musculoskeletal Abnormalities .
C16.131.621.207 Craniofacial Abnormalities .
C16.131.621.207.207 Cleidocranial Dysplasia .
C16.131.621.207.231 Craniofacial Dysostosis .
C16.131.621.207.231.576 Mandibulofacial Dysostosis .
C23 Pathological Conditions, Signs and Symptoms .
C23.888 Signs and Symptoms .
C23.888.592 Neurologic Manifestations .
C23.888.592.763 Sensation Disorders .
C23.888.592.763.550 Olfaction Disorders .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Dysostoses .
Dysostosis .
Defective bone formation involving individual bones, singly or in combination. .
1.00
15333
 
Craniofacial Dysostosis .
Craniofacial Dysarthrosis .
Craniofacial Dysostosis Syndrome .
Craniofacial Dysostosis Type 1 .
Craniofacial Dysostosis, Type I .
Crouzon Craniofacial Dysostosis .
Crouzon Disease .
Crouzon Syndrome .
Craniofacial Dysarthroses .
Craniofacial Dysostoses .
Craniofacial Dysostosis Syndromes .
Craniofacial Dysostosis, Crouzon .
Crouzons Disease .
Dysarthroses, Craniofacial .
Dysarthrosis, Craniofacial .
Dysostoses, Craniofacial .
Dysostosis, Craniofacial .
Crouzon's Disease .
Autosomal dominant CRANIOSYNOSTOSIS with shallow ORBITS; EXOPHTHALMOS; and maxillary hypoplasia. .
0.66
792233
 
Olfaction Disorders .
Cacosmia .
Dysosmia .
Cacosmias .
Dysosmias .
Olfaction Disorder .
Paraosmias .
Smell Disorder .
Anosmia .
Smell Disorders .
Paraosmia .
Loss of or impaired ability to smell. This may be caused by OLFACTORY NERVE DISEASES; PARANASAL SINUS DISEASES; viral RESPIRATORY TRACT INFECTIONS; CRANIOCEREBRAL TRAUMA; SMOKING; and other conditions. .
0.65
603456
 
Cleidocranial Dysplasia .
Cleidocranial Digital Dysostosis .
Marie-Sainton Syndrome .
Scheuthauer-Marie-Sainton Syndrome .
Cleidocranial Digital Dysostoses .
Cleidocranial Dysostoses .
Cleidocranial Dysplasias .
Dysostoses, Cleidocranial .
Dysostoses, Cleidocranial Digital .
Dysostosis, Cleidocranial Digital .
Dysplasia, Cleidocranial .
Dysplasias, Cleidocranial .
Marie Sainton Syndrome .
Scheuthauer Marie Sainton Syndrome .
Syndrome, Marie-Sainton .
Syndrome, Scheuthauer-Marie-Sainton .
Cleidocranial Dysostosis .
Dysostosis, Cleidocranial .
Autosomal dominant syndrome in which there is delayed closing of the CRANIAL FONTANELLES; complete or partial absence of the collarbones (CLAVICLES); wide PUBIC SYMPHYSIS; short middle phalanges of the fifth fingers; and dental and vertebral anomalies. .
0.64
52739
 
Mandibulofacial Dysostosis .
Franceschetti-Zwahlen-Klein Syndrome .
Mandibulofacial Dysostosis (MFD1) .
Treacher Collins-Franceschetti Syndrome .
Collins Syndrome, Treacher .
Dysostoses, Mandibulofacial .
Dysostosis, Mandibulofacial .
Mandibulofacial Dysostoses .
Syndrome, Treacher Collins .
Treacher Collins Syndrome .
A hereditary disorder occurring in two forms: the complete form (Franceschetti's syndrome) is characterized by antimongoloid slant of the palpebral fissures, coloboma of the lower lid, micrognathia and hypoplasia of the zygomatic arches, and microtia. It is transmitted as an autosomal trait. The incomplete form (Treacher Collins syndrome) is characterized by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected. (Dorland, 27th ed) .
0.63
441431