Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3316404014 | Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3316405010 | Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3316406011 | Cardiogenital syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3316407019 | Malouf syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3316408012 | Najjar syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 754201000241114 | syndrome de cardiomyopathie dilatée-hypogonadisme hypergonadotrope (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 909721000172119 | syndrome cardiogénital | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 946591000172112 | syndrome de cardiomyopathie dilatée-hypogonadisme hypergonadotrope | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3316409016 | Syndrome that associates dilated cardiomyopathy with hypergonadotropic hypogonadism. Prevalence is unknown but less than 20 affected families have been described in the literature so far. Occasional findings include a broad nasal base, blepharoptosis, mild intellectual deficit, mild skeletal anomalies and metabolic abnormalities. Mutations in the LMNA gene were recently detected in two sisters with an overlapping clinical phenotype but with additional findings that included a narrow chest, sloping shoulders, aged appearance of the hands and feet and facial dysmorphism (beaked nose and severe retrognathia). Transmission appears to be autosomal recessive. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | est un(e) (attribut) | Developmental hereditary disorder | true | Inferred relationship | Some | ||
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | est un(e) (attribut) | Congenital anomaly of myocardium | true | Inferred relationship | Some | ||
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | est un(e) (attribut) | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | est un(e) (attribut) | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | est un(e) (attribut) | Reproductive system hereditary disorder | true | Inferred relationship | Some | ||
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | est un(e) (attribut) | Primary hypogonadism (disorder) | true | Inferred relationship | Some | ||
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | est un(e) (attribut) | Congestive cardiomyopathy (disorder) | true | Inferred relationship | Some | ||
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | localisation d'une constatation (attribut) | Gonadal endocrine structure | false | Inferred relationship | Some | ||
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | morphologie associée (attribut) | dilatation | false | Inferred relationship | Some | 2 | |
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | localisation d'une constatation (attribut) | structure du myocarde | false | Inferred relationship | Some | 2 | |
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 3 | |
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | morphologie associée (attribut) | dilatation | true | Inferred relationship | Some | 1 | |
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | localisation d'une constatation (attribut) | structure du myocarde | true | Inferred relationship | Some | 1 | |
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | localisation d'une constatation (attribut) | Gonadal endocrine structure | true | Inferred relationship | Some | 3 | |
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) | est un(e) (attribut) | Congenital cardiovascular disorder (disorder) | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR