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723308003: Epidermolysis bullosa simplex with muscular dystrophy (disorder)


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
3424003010 Epidermolysis bullosa simplex with muscular dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3424004016 Epidermolysis bullosa simplex with muscular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3424005015 Limb girdle muscular dystrophy with epidermolysis bullosa simplex en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5402999013 A form of epidermolysis bullosa simplex (EBS) characterized by generalized blistering associated with muscular dystrophy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403000014 A form of epidermolysis bullosa simplex (EBS) characterised by generalised blistering associated with muscular dystrophy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3424003010 Epidermolysis bullosa simplex with muscular dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3424004016 Epidermolysis bullosa simplex with muscular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3424005015 Limb girdle muscular dystrophy with epidermolysis bullosa simplex en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3424006019 A basal subtype of epidermolysis bullosa simplex characterized by generalized blistering associated with muscular dystrophy. Onset of blistering is usually as early as birth, muscular dystrophy manifests between infancy and adulthood. Blisters are often hemorrhagic and heal with mild atrophic scarring and rare milia formation. Associated findings comprise markedly dystrophic nails, and focal keratoderma of the palms and soles. Extracutaneous involvement is usually present. Caused by mutations in the PLEC gene (8q24) encoding plectin. Plectin deficiency can be demonstrated in skin and muscle by analysis with specific antibodies. Transmission is autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3424007011 A basal subtype of epidermolysis bullosa simplex characterised by generalised blistering associated with muscular dystrophy. Onset of blistering is usually as early as birth, muscular dystrophy manifests between infancy and adulthood. Blisters are often haemorrhagic and heal with mild atrophic scarring and rare milia formation. Associated findings comprise markedly dystrophic nails, and focal keratoderma of the palms and soles. Extracutaneous involvement is usually present. Caused by mutations in the PLEC gene (8q24) encoding plectin. Plectin deficiency can be demonstrated in skin and muscle by analysis with specific antibodies. Transmission is autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402999013 A form of epidermolysis bullosa simplex (EBS) characterized by generalized blistering associated with muscular dystrophy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403000014 A form of epidermolysis bullosa simplex (EBS) characterised by generalised blistering associated with muscular dystrophy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3425791001000116 Epidermolysis bullosa simplex mit Muskeldystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
874911000172110 dystrophie musculaire des ceintures associée à une épidermolyse bulleuse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
982371000172112 epidermolyse bulleuse simple avec dystrophie musculaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
874911000172110 dystrophie musculaire des ceintures associée à une épidermolyse bulleuse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
982371000172112 epidermolyse bulleuse simple avec dystrophie musculaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3425791001000116 Epidermolysis bullosa simplex mit Muskeldystrophie 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
Epidermolysis bullosa simplex with muscular dystrophy Is a Autosomal recessive muscular dystrophy with limb girdle distribution (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Epidermolysis bullosa simplex with muscular dystrophy Is a Musculoskeletal and connective tissue disorder (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Epidermolysis bullosa simplex with muscular dystrophy Is a Basal epidermolysis bullosa simplex (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Epidermolysis bullosa simplex with muscular dystrophy Finding site Connective tissue structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Epidermolysis bullosa simplex with muscular dystrophy Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 5
Epidermolysis bullosa simplex with muscular dystrophy Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 6
Epidermolysis bullosa simplex with muscular dystrophy Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 7
Epidermolysis bullosa simplex with muscular dystrophy Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 7
Epidermolysis bullosa simplex with muscular dystrophy Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 7
Epidermolysis bullosa simplex with muscular dystrophy Associated morphology Epidermolysis (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 5
Epidermolysis bullosa simplex with muscular dystrophy Finding site Stratum germinativum false Inferred relationship Existential restriction modifier (core metadata concept) 5
Epidermolysis bullosa simplex with muscular dystrophy Associated morphology Dystrophy false Inferred relationship Existential restriction modifier (core metadata concept) 6
Epidermolysis bullosa simplex with muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 6
Epidermolysis bullosa simplex with muscular dystrophy Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Epidermolysis bullosa simplex with muscular dystrophy Is a Congenital anomaly of skeletal muscle (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Epidermolysis bullosa simplex with muscular dystrophy Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Epidermolysis bullosa simplex with muscular dystrophy Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Epidermolysis bullosa simplex with muscular dystrophy Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Epidermolysis bullosa simplex with muscular dystrophy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 2
Epidermolysis bullosa simplex with muscular dystrophy Finding site Stratum germinativum true Inferred relationship Existential restriction modifier (core metadata concept) 1
Epidermolysis bullosa simplex with muscular dystrophy Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Epidermolysis bullosa simplex with muscular dystrophy Associated morphology Epidermolysis (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Epidermolysis bullosa simplex with muscular dystrophy Is a Chronic disease of skin true Inferred relationship Existential restriction modifier (core metadata concept)
Epidermolysis bullosa simplex with muscular dystrophy Is a Congenital hereditary muscular dystrophy true Inferred relationship Existential restriction modifier (core metadata concept)
Epidermolysis bullosa simplex with muscular dystrophy Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 3
Epidermolysis bullosa simplex with muscular dystrophy Is a Autosomal recessive epidermolysis bullosa simplex 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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