Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
3304690010 |
Cranio-facio-digito-genital syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3304691014 |
Harrod syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
3304693012 |
Craniofacial digital and genital anomalies syndrome (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
3304694018 |
Craniofacial digital and genital anomalies syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
6611791000146110 |
Harrod-syndroom |
nl |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT Netherlands NRC maintained module (core metadata concept) |
6611801000146114 |
syndroom van Harrod |
nl |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT Netherlands NRC maintained module (core metadata concept) |
6748141000146111 |
syndroom van craniofaciale, digitale en genitale anomalieën |
nl |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT Netherlands NRC maintained module (core metadata concept) |
8270871000146111 |
cranio-facio-digito-genitaal-syndroom |
nl |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT Netherlands NRC maintained module (core metadata concept) |
8270881000146113 |
syndroom van craniofaciale, digitale en genitale afwijkingen |
nl |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT Netherlands NRC maintained module (core metadata concept) |
8270891000146110 |
syndroom van craniofaciale, digitale en genitale afwijkingen (aandoening) |
nl |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT Netherlands NRC maintained module (core metadata concept) |
3304692019 |
The association of intellectual deficit, facial dysmorphism (a highly arched palate, pointed chin, and small mouth, hypotelorism, a long nose and large protruding ears), arachnodactyly, hypogenitalism (undescended testes and hypospadias) and failure to thrive. So far, it has been described in three males (including two brothers). An autosomal recessive mode of transmission has been suggested. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |