Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3308843016 | Hereditary hypotrichosis simplex of scalp (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3308849017 | Hereditary hypotrichosis simplex of scalp | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3308850017 | Hypotrichosis simplex of scalp | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5401529013 | Hypotrichosis simplex of the scalp (HSS) is characterized by diffuse progressive hair loss that is confined to the scalp. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401530015 | Hypotrichosis simplex of the scalp (HSS) is characterised by diffuse progressive hair loss that is confined to the scalp. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3308843016 | Hereditary hypotrichosis simplex of scalp (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3308843016 | Hereditary hypotrichosis simplex of scalp (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3308849017 | Hereditary hypotrichosis simplex of scalp | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3308849017 | Hereditary hypotrichosis simplex of scalp | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3308850017 | Hypotrichosis simplex of scalp | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3308850017 | Hypotrichosis simplex of scalp | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3309176013 | Hypotrichosis simplex of the scalp (HSS) has manifestation of diffuse progressive hair loss that is confined to the scalp. Prevalence is unknown but HSS has been described in multiple members (males and females) of several large families. Progressive hair loss generally begins during the first decade of life and most patients are completely bald by the third decade of life. Body, axillary and facial hair, as well as the eyebrows and eyelashes are unaffected. There are no anomalies of the skin, nails and teeth. The causative gene CDSN (encoding the keratinocyte adhesion molecule, corneodesmosin) has been mapped to chromosome 6p21.3. Transmitted in an autosomal dominant manner. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401529013 | Hypotrichosis simplex of the scalp (HSS) is characterized by diffuse progressive hair loss that is confined to the scalp. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401530015 | Hypotrichosis simplex of the scalp (HSS) is characterised by diffuse progressive hair loss that is confined to the scalp. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3439541001000116 | Hypotrichosis simplex des Skalps | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6276031000241111 | hypotrichose héréditaire simple du cuir chevelu | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6276041000241118 | HS (hypotrichose simple) du 'scalp' | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6276031000241111 | hypotrichose héréditaire simple du cuir chevelu | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6276041000241118 | HS (hypotrichose simple) du 'scalp' | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3439541001000116 | Hypotrichosis simplex des Skalps | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hypotrichosis simplex of the scalp (HSS) is characterized by diffuse progressive hair loss that is confined to the scalp. | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Hypotrichosis simplex of the scalp (HSS) is characterized by diffuse progressive hair loss that is confined to the scalp. | Is a | Hypotrichosis (disorder) | false | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Hypotrichosis simplex of the scalp (HSS) is characterized by diffuse progressive hair loss that is confined to the scalp. | Is a | Disorder of scalp | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Hypotrichosis simplex of the scalp (HSS) is characterized by diffuse progressive hair loss that is confined to the scalp. | Is a | Hereditary disorder of the integument (disorder) | false | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Hypotrichosis simplex of the scalp (HSS) is characterized by diffuse progressive hair loss that is confined to the scalp. | Is a | Disorder of skin of head (disorder) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Hypotrichosis simplex of the scalp (HSS) is characterized by diffuse progressive hair loss that is confined to the scalp. | Finding site | Skin of scalp | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 2 | |
Hypotrichosis simplex of the scalp (HSS) is characterized by diffuse progressive hair loss that is confined to the scalp. | Finding site | Hair structure (body structure) | false | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Hypotrichosis simplex of the scalp (HSS) is characterized by diffuse progressive hair loss that is confined to the scalp. | Is a | Hereditary hypotrichosis simplex | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Hypotrichosis simplex of the scalp (HSS) is characterized by diffuse progressive hair loss that is confined to the scalp. | Associated morphology | Growth alteration | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Hypotrichosis simplex of the scalp (HSS) is characterized by diffuse progressive hair loss that is confined to the scalp. | Finding site | Hair structure (body structure) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)