719432000: Late-onset junctional epidermolysis bullosa (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\...

\Degenerative skin disorder\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa

\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa

\General finding of soft tissue\Skin finding\Disorder of skin\Degenerative skin disorder\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\General finding of soft tissue\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\Integumentary system finding\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\Integumentary system finding\Skin finding\Disorder of skin\Degenerative skin disorder\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\Integumentary system finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\Disease\Degenerative disorder\Degenerative skin disorder\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\Disease\Disorder of body system\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\Disease\Congenital disease\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\Disease\Developmental disorder\Developmental hereditary disorder\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa
\Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Junctional epidermolysis bullosa\Late-onset junctional epidermolysis bullosa

Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3316324014 Late-onset junctional epidermolysis bullosa (disorder) en Fully specified name Active Case insensitive SNOMED CT core

3316325010 Late-onset junctional epidermolysis bullosa en Synonym Active Case insensitive SNOMED CT core

3316326011 A subtype of junctional epidermolysis bullosa the condition occurs in childhood or young adulthood. 22 patients in 12 families have been reported to date. Blistering occurs at first around nails, accompanied by nail dystrophy and shedding, and then affects the hands and feet and, to a lesser extent, the elbows, knees, along with atrophic scarring. Other manifestations include disappearance of dermatoglyphs and palmoplantar hyperhidrosis. Extracutaneous involvement is restricted to soft tissue abnormalities of the oral cavity and enamel defects with development of caries. COL17A1 mutations have recently been described in an affected family. The condition follows an autosomal recessive pattern of inheritance. en Definition Active Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Late-onset junctional epidermolysis bullosa	Occurrence	Congenital	true	Inferred relationship	Some	1
Late-onset junctional epidermolysis bullosa	Pathological process	Pathological developmental process	true	Inferred relationship	Some	1
Late-onset junctional epidermolysis bullosa	Associated morphology	Epidermolysis	true	Inferred relationship	Some	1
Late-onset junctional epidermolysis bullosa	Finding site	Skin structure	true	Inferred relationship	Some	1
Late-onset junctional epidermolysis bullosa	Is a	Autosomal recessive hereditary disorder	false	Inferred relationship	Some
Late-onset junctional epidermolysis bullosa	Is a	Inherited disorder of connective tissue	false	Inferred relationship	Some
Late-onset junctional epidermolysis bullosa	Is a	Hereditary disorder of the integument	false	Inferred relationship	Some
Late-onset junctional epidermolysis bullosa	Is a	Junctional epidermolysis bullosa	true	Inferred relationship	Some
Late-onset junctional epidermolysis bullosa	Finding site	Connective tissue structure	false	Inferred relationship	Some
Late-onset junctional epidermolysis bullosa	Finding site	Skin structure	false	Inferred relationship	Some	3
Late-onset junctional epidermolysis bullosa	Finding site	Skin structure	false	Inferred relationship	Some	4
Late-onset junctional epidermolysis bullosa	Associated morphology	Developmental abnormality	false	Inferred relationship	Some	3
Late-onset junctional epidermolysis bullosa	Occurrence	Congenital	false	Inferred relationship	Some	3
Late-onset junctional epidermolysis bullosa	Associated morphology	Epidermolysis	false	Inferred relationship	Some	4

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3316324014	Late-onset junctional epidermolysis bullosa (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3316325010	Late-onset junctional epidermolysis bullosa	en	Synonym	Active	Case insensitive	SNOMED CT core
3316326011	A subtype of junctional epidermolysis bullosa the condition occurs in childhood or young adulthood. 22 patients in 12 families have been reported to date. Blistering occurs at first around nails, accompanied by nail dystrophy and shedding, and then affects the hands and feet and, to a lesser extent, the elbows, knees, along with atrophic scarring. Other manifestations include disappearance of dermatoglyphs and palmoplantar hyperhidrosis. Extracutaneous involvement is restricted to soft tissue abnormalities of the oral cavity and enamel defects with development of caries. COL17A1 mutations have recently been described in an affected family. The condition follows an autosomal recessive pattern of inheritance.	en	Definition	Active	Case sensitive	SNOMED CT core