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 |
| 3315795011 | Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3315799017 | Primary hypergonadotropic hypogonadism and partial alopecia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3315800018 | Al Awadi Farag Teebi syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 753961000241116 | syndrome d'hypogonadisme hypergonadotrope primaire-alopécie partielle (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 888741000172113 | syndrome d'Al Awadi-Farag-Teebi | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 908031000172113 | syndrome d'hypogonadisme hypergonadotrope primaire-alopécie partielle | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3315801019 | This syndrome is characterized by primary hypergonadotropic hypogonadism and partial alopecia. So far, it has been described in seven patients from three families. Mullerian hypoplasia, absent or streak ovaries, hypoplastic internal genitalia and primary amenorrhea were described in the females. The male appeared to have germinal cell aplasia. All patients displayed partial scalp alopecia, and axillary and pubic hair was sparse or absent in the females but normal in the male patient. Additional findings in some of the female patients included sparse eyebrows, microcephaly, flat occiput, dorsal kyphosis and mild intellectual deficit. Transmission was autosomal recessive. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3315802014 | This syndrome is characterised by primary hypergonadotropic hypogonadism and partial alopecia. So far, it has been described in seven patients from three families. Mullerian hypoplasia, absent or streak ovaries, hypoplastic internal genitalia and primary amenorrhoea were described in the females. The male appeared to have germinal cell aplasia. All patients displayed partial scalp alopecia, and axillary and pubic hair was sparse or absent in the females but normal in the male patient. Additional findings in some of the female patients included sparse eyebrows, microcephaly, flat occiput, dorsal kyphosis and mild intellectual deficit. Transmission was autosomal recessive. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) | est un(e) (attribut) | Congenital disease | false | Inferred relationship | Some | ||
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) | localisation d'une constatation (attribut) | Gonadal endocrine structure | true | Inferred relationship | Some | 2 | |
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) | est un(e) (attribut) | Partial loss of hair | true | Inferred relationship | Some | ||
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) | est un(e) (attribut) | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) | est un(e) (attribut) | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) | est un(e) (attribut) | Reproductive system hereditary disorder | true | Inferred relationship | Some | ||
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) | est un(e) (attribut) | Primary hypogonadism (disorder) | true | Inferred relationship | Some | ||
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) | localisation d'une constatation (attribut) | Gonadal endocrine structure | false | Inferred relationship | Some | ||
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) | morphologie associée (attribut) | Absence (morphologic abnormality) | false | Inferred relationship | Some | 2 | |
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) | localisation d'une constatation (attribut) | Hair structure (body structure) | false | Inferred relationship | Some | 2 | |
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) | morphologie associée (attribut) | Absence (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 1 | |
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) | localisation d'une constatation (attribut) | Hair structure (body structure) | true | Inferred relationship | Some | 1 | |
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 3 | |
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) | localisation d'une constatation (attribut) | Gonadal endocrine structure | false | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR