Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3429742015 | Autosomal recessive posterior column ataxia and retinitis pigmentosa (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3429743013 | Autosomal recessive posterior column ataxia and retinitis pigmentosa | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3429744019 | Posterior column ataxia with retinitis pigmentosa syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5403206013 | Posterior column ataxia - retinitis pigmentosa is characterized by the association of progressive sensory ataxia and retinitis pigmentosa. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403207016 | Posterior column ataxia - retinitis pigmentosa is characterised by the association of progressive sensory ataxia and retinitis pigmentosa. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3429742015 | Autosomal recessive posterior column ataxia and retinitis pigmentosa (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3429743013 | Autosomal recessive posterior column ataxia and retinitis pigmentosa | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3429744019 | Posterior column ataxia with retinitis pigmentosa syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3429745018 | Syndrome that is characterized by the association of progressive sensory ataxia and retinitis pigmentosa. Around 20 cases have been described in the last 50 years. Onset of symptoms usually occurs in childhood. The clinical picture is progressive, homogenous and includes severe sensory ataxia, proprioceptive loss (affecting the iliac crest, upper limbs and thorax), generalized areflexia and diffuse pigmentary retinopathy leading to blindness. Scoliosis, camptodactyly, achalasia and/or gastrointestinal motility dysfunction may also be present. The disease is associated with degeneration of the posterior column of the spinal cord. The causative gene, FLVCR1 (1q32.3), has been identified and localized to the AXPC1 locus (1q32-q31). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3429746017 | Syndrome that is characterised by the association of progressive sensory ataxia and retinitis pigmentosa. Around 20 cases have been described in the last 50 years. Onset of symptoms usually occurs in childhood. The clinical picture is progressive, homogenous and includes severe sensory ataxia, proprioceptive loss (affecting the iliac crest, upper limbs and thorax), generalised areflexia and diffuse pigmentary retinopathy leading to blindness. Scoliosis, camptodactyly, achalasia and/or gastrointestinal motility dysfunction may also be present. The disease is associated with degeneration of the posterior column of the spinal cord. The causative gene, FLVCR1 (1q32.3), has been identified and localised to the AXPC1 locus (1q32-q31). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403206013 | Posterior column ataxia - retinitis pigmentosa is characterized by the association of progressive sensory ataxia and retinitis pigmentosa. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403207016 | Posterior column ataxia - retinitis pigmentosa is characterised by the association of progressive sensory ataxia and retinitis pigmentosa. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
602741000274112 | Hinterstrangataxie und Retinitis pigmentosa, autosomal-rezessive Form | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3442701001000118 | Hinterstrangataxie - Retinitis pigmentosa | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5787091000241112 | ataxie du cordon postérieur et rétinite pigmentaire autosomique récessive | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5787091000241112 | ataxie du cordon postérieur et rétinite pigmentaire autosomique récessive | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
602741000274112 | Hinterstrangataxie und Retinitis pigmentosa, autosomal-rezessive Form | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3442701001000118 | Hinterstrangataxie - Retinitis pigmentosa | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)