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763630007: Satoyoshi syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3643093010 Satoyoshi syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3643095015 Komuragaeri disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3643097011 Satoyoshi syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404123016 Satoyoshi syndrome is a rare, multisystemic autoimmune disease mainly characterized by intermittent painful muscle spasms, alopecia (totalis or universalis in most cases) and long-lasting diarrhea that could lead to malnutrition, growth retardation, and amenorrhea. Secondary bone deformities and various endocrine anomalies may also be associated. Antinuclear antibodies are reported in many cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404124010 Satoyoshi syndrome is a rare, multisystemic autoimmune disease mainly characterised by intermittent painful muscle spasms, alopecia (totalis or universalis in most cases) and long-lasting diarrhoea that could lead to malnutrition, growth retardation, and amenorrhoea. Secondary bone deformities and various endocrine anomalies may also be associated. Antinuclear antibodies are reported in many cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3643093010 Satoyoshi syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3643095015 Komuragaeri disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3643097011 Satoyoshi syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3643094016 A rare multisystemic autoimmune disease mainly characterized by intermittent painful muscle spasms, alopecia (totalis or universalis in most cases) and long-lasting diarrhea that could lead to malnutrition, growth retardation, and amenorrhea. Secondary bone deformities and various endocrine anomalies may also be associated. Antinuclear antibodies are reported in many cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3643096019 A rare multisystemic autoimmune disease mainly characterised by intermittent painful muscle spasms, alopecia (totalis or universalis in most cases) and long-lasting diarrhoea that could lead to malnutrition, growth retardation, and amenorrhoea. Secondary bone deformities and various endocrine anomalies may also be associated. Antinuclear antibodies are reported in many cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404123016 Satoyoshi syndrome is a rare, multisystemic autoimmune disease mainly characterized by intermittent painful muscle spasms, alopecia (totalis or universalis in most cases) and long-lasting diarrhea that could lead to malnutrition, growth retardation, and amenorrhea. Secondary bone deformities and various endocrine anomalies may also be associated. Antinuclear antibodies are reported in many cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404124010 Satoyoshi syndrome is a rare, multisystemic autoimmune disease mainly characterised by intermittent painful muscle spasms, alopecia (totalis or universalis in most cases) and long-lasting diarrhoea that could lead to malnutrition, growth retardation, and amenorrhoea. Secondary bone deformities and various endocrine anomalies may also be associated. Antinuclear antibodies are reported in many cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3431401001000118 Satoyoshi-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
981051000172110 syndrome de Satoyoshi fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
981051000172110 syndrome de Satoyoshi fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3431401001000118 Satoyoshi-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Satoyoshi syndrome (disorder) Is a Alopecia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Satoyoshi syndrome (disorder) Is a Autoimmune disease false Inferred relationship Existential restriction modifier (core metadata concept)
Satoyoshi syndrome (disorder) Is a Disease of intestine true Inferred relationship Existential restriction modifier (core metadata concept)
Satoyoshi syndrome (disorder) Pathological process (attribute) Autoimmune process true Inferred relationship Existential restriction modifier (core metadata concept) 2
Satoyoshi syndrome (disorder) Finding site Intestinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Satoyoshi syndrome (disorder) Associated morphology Absence (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Satoyoshi syndrome (disorder) Pathological process (attribute) Autoimmune process true Inferred relationship Existential restriction modifier (core metadata concept) 1
Satoyoshi syndrome (disorder) Finding site Hair structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Satoyoshi syndrome (disorder) Is a Autoimmune skin disease true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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