Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
3320701011 |
Acrofacial dysostosis Catania type (disorder) |
en |
Fully specified name |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
3320702016 |
Acrofacial dysostosis Catania type |
en |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
3320703014 |
Opitz Caltabiano syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3320704015 |
A very rare type of acrofacialdysostosis with characteristics of mild intrauterine growth retardation, postnatal short stature, microcephaly, widow's peak, mandibulofacial dysostosis without cleft palate, frequent caries, mild pre and postaxial limb hypoplasia with brachydactyly, mild interdigital webbing, simian creases, inguinal hernia and cryptorchidism and hypospadias in males. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
899781000172112 |
dysostose acrofaciale type Catane |
fr |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
Belgian module (core metadata concept) |
1012641000172117 |
syndrome d'Opitz-Caltabiano |
fr |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
Belgian module (core metadata concept) |
878581000172118 |
acrofaciale dysostose, Catania-type |
nl |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
Belgian module (core metadata concept) |
953381000172110 |
syndroom van Opitz-Caltabiano |
nl |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
Belgian module (core metadata concept) |