723553000: Transient bullous dermolysis of newborn (disorder)

SNOMED CT Concept\Clinical finding\...

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

\Degenerative skin disorder\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn

\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn

\Acute skin disorder\Transient bullous dermolysis of newborn

\General finding of soft tissue\Skin finding\Disorder of skin\Degenerative skin disorder\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\General finding of soft tissue\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\General finding of soft tissue\Skin finding\Disorder of skin\Acute skin disorder\Transient bullous dermolysis of newborn
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\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\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Acute skin disorder\Transient bullous dermolysis of newborn

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Acute skin disorder\Transient bullous dermolysis of newborn
\Integumentary system finding\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\Integumentary system finding\Skin finding\Disorder of skin\Degenerative skin disorder\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\Integumentary system finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\Integumentary system finding\Skin finding\Disorder of skin\Acute skin disorder\Transient bullous dermolysis of newborn

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Transient bullous dermolysis of newborn
\Disease\Degenerative disorder\Degenerative skin disorder\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\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\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Acute skin disorder\Transient bullous dermolysis of newborn
\Disease\Disorder of body system\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\Disease\Congenital disease\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Acute skin disorder\Transient bullous dermolysis of newborn
\Disease\Developmental disorder\Developmental hereditary disorder\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Epidermolysis bullosa\Dystrophic epidermolysis bullosa\Generalised dystrophic epidermolysis bullosa\Transient bullous dermolysis of newborn
\Disease\Acute disease\Acute skin disorder\Transient bullous dermolysis of newborn

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

Descriptions:

Id Description Lang Type Status Case? Module

3425082010 Transient bullous dermolysis of newborn (disorder) en Fully specified name Active Case insensitive SNOMED CT core

3425083017 Transient bullous dermolysis of newborn en Synonym Active Case insensitive SNOMED CT core

3425084011 A rare subtype of dystrophic epidermolysis bullosa characterized by generalized blistering at birth that usually regresses within the first 6 to 24 months of life. Less than 30 cases have been reported to date. The disease usually manifests at birth. Skin blisters generally affect the whole body. Blisters can also affect the oral cavity. Disease activity usually ceases within the first 6 to 24 months of life. However, nail dystrophy and some degree of skin fragility can persist in adulthood. Caused by mutations within the type VII collagen gene (COL7A1). Mutations in this gene lead to reduced amounts or an alteration in function of collagen VII. The condition is usually inherited in an autosomal dominant manner, but can also rarely be transmitted as an autosomal recessive trait. en Definition Active Case sensitive SNOMED CT core

3425085012 A rare subtype of dystrophic epidermolysis bullosa characterised by generalised blistering at birth that usually regresses within the first 6 to 24 months of life. Less than 30 cases have been reported to date. The disease usually manifests at birth. Skin blisters generally affect the whole body. Blisters can also affect the oral cavity. Disease activity usually ceases within the first 6 to 24 months of life. However, nail dystrophy and some degree of skin fragility can persist in adulthood. Caused by mutations within the type VII collagen gene (COL7A1). Mutations in this gene lead to reduced amounts or an alteration in function of collagen VII. The condition is usually inherited in an autosomal dominant manner, but can also rarely be transmitted as an autosomal recessive trait. en Definition Active Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Transient bullous dermolysis of newborn	Occurrence	Congenital	true	Inferred relationship	Some	2
Transient bullous dermolysis of newborn	Finding site	Skin structure	true	Inferred relationship	Some	2
Transient bullous dermolysis of newborn	Pathological process	Pathological developmental process	false	Inferred relationship	Some	1
Transient bullous dermolysis of newborn	Associated morphology	Epidermolysis	false	Inferred relationship	Some	1
Transient bullous dermolysis of newborn	Clinical course	Transitory	false	Inferred relationship	Some	1
Transient bullous dermolysis of newborn	Pathological process	Pathological developmental process	true	Inferred relationship	Some	2
Transient bullous dermolysis of newborn	Finding site	Skin structure	false	Inferred relationship	Some	1
Transient bullous dermolysis of newborn	Associated morphology	Epidermolysis	true	Inferred relationship	Some	2
Transient bullous dermolysis of newborn	Occurrence	Neonatal	false	Inferred relationship	Some	1
Transient bullous dermolysis of newborn	Is a	Neonatal dermatosis	false	Inferred relationship	Some
Transient bullous dermolysis of newborn	Clinical course	Transitory	true	Inferred relationship	Some	3
Transient bullous dermolysis of newborn	Is a	Autosomal hereditary disorder	true	Inferred relationship	Some
Transient bullous dermolysis of newborn	Is a	Neonatal disorder	false	Inferred relationship	Some
Transient bullous dermolysis of newborn	Is a	Acute skin disorder	true	Inferred relationship	Some
Transient bullous dermolysis of newborn	Is a	Acute metabolic disorder	false	Inferred relationship	Some
Transient bullous dermolysis of newborn	Is a	Generalised dystrophic epidermolysis bullosa	true	Inferred relationship	Some
Transient bullous dermolysis of newborn	Is a	Inherited disorder of connective tissue	false	Inferred relationship	Some
Transient bullous dermolysis of newborn	Is a	Hereditary disorder of the integument	false	Inferred relationship	Some
Transient bullous dermolysis of newborn	Finding site	Connective tissue structure	false	Inferred relationship	Some
Transient bullous dermolysis of newborn	Finding site	Skin structure	false	Inferred relationship	Some	4
Transient bullous dermolysis of newborn	Finding site	Skin structure	false	Inferred relationship	Some	5
Transient bullous dermolysis of newborn	Associated morphology	Epidermolysis	false	Inferred relationship	Some	4
Transient bullous dermolysis of newborn	Occurrence	Neonatal	false	Inferred relationship	Some	4
Transient bullous dermolysis of newborn	Clinical course	Transitory	false	Inferred relationship	Some	4
Transient bullous dermolysis of newborn	Associated morphology	Developmental abnormality	false	Inferred relationship	Some	5
Transient bullous dermolysis of newborn	Occurrence	Congenital	false	Inferred relationship	Some	5
Transient bullous dermolysis of newborn	Is a	Neonatal metabolic disorder	false	Inferred relationship	Some

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
3425082010	Transient bullous dermolysis of newborn (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3425083017	Transient bullous dermolysis of newborn	en	Synonym	Active	Case insensitive	SNOMED CT core
3425084011	A rare subtype of dystrophic epidermolysis bullosa characterized by generalized blistering at birth that usually regresses within the first 6 to 24 months of life. Less than 30 cases have been reported to date. The disease usually manifests at birth. Skin blisters generally affect the whole body. Blisters can also affect the oral cavity. Disease activity usually ceases within the first 6 to 24 months of life. However, nail dystrophy and some degree of skin fragility can persist in adulthood. Caused by mutations within the type VII collagen gene (COL7A1). Mutations in this gene lead to reduced amounts or an alteration in function of collagen VII. The condition is usually inherited in an autosomal dominant manner, but can also rarely be transmitted as an autosomal recessive trait.	en	Definition	Active	Case sensitive	SNOMED CT core
3425085012	A rare subtype of dystrophic epidermolysis bullosa characterised by generalised blistering at birth that usually regresses within the first 6 to 24 months of life. Less than 30 cases have been reported to date. The disease usually manifests at birth. Skin blisters generally affect the whole body. Blisters can also affect the oral cavity. Disease activity usually ceases within the first 6 to 24 months of life. However, nail dystrophy and some degree of skin fragility can persist in adulthood. Caused by mutations within the type VII collagen gene (COL7A1). Mutations in this gene lead to reduced amounts or an alteration in function of collagen VII. The condition is usually inherited in an autosomal dominant manner, but can also rarely be transmitted as an autosomal recessive trait.	en	Definition	Active	Case sensitive	SNOMED CT core