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119181002: Skin part (body structure)

SNOMED CT Concept\Body structure (body structure)\Anatomical or acquired body structure (body structure)\Anatomical structure\...

\An anatomical structure that consists of the maximal set of organ parts so connected to one another that together they constitute a self-contained unit of macroscopic anatomy, distinct both morphologically and functionally from other such units. Together with other organs, an organ constitutes an organ system or a body part. An organ is divisible into organ parts but not organs (examples: femur, biceps, liver, heart, aorta, sciatic nerve, ovary).\Organ part\Skin part
\An anatomical structure that consists of the maximal set of organ parts so connected to one another that together they constitute a self-contained unit of macroscopic anatomy, distinct both morphologically and functionally from other such units. Together with other organs, an organ constitutes an organ system or a body part. An organ is divisible into organ parts but not organs (examples: femur, biceps, liver, heart, aorta, sciatic nerve, ovary).\Skin structure\Skin part

\Body tissue structure\Structure of soft tissue (body structure)\Skin and/or subcutaneous tissue structure (body structure)\Skin structure\Skin part

\Body region structure\Skin and/or subcutaneous tissue structure (body structure)\Skin structure\Skin part

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

452148019 Skin part en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

705299011 Skin part (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Skin part	Is a	Organ part	true	Inferred relationship	Some
Skin part	Is a	Skin structure	true	Inferred relationship	Some
Skin part	partie de	Entire skin	false	Additional relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Coronet	Is a	False	Skin part	Inferred relationship	Some
Structure of toruli tactiles (body structure)	Is a	True	Skin part	Inferred relationship	Some
Hoof part	Is a	False	Skin part	Inferred relationship	Some
Structure of skin region	Is a	True	Skin part	Inferred relationship	Some
Sweat gland duct structure	Is a	False	Skin part	Inferred relationship	Some
Dander	Is a	False	Skin part	Inferred relationship	Some
Velvet of antler	Is a	False	Skin part	Inferred relationship	Some
Chestnut structure	Is a	False	Skin part	Inferred relationship	Some
Dermis structure	Is a	True	Skin part	Inferred relationship	Some
Cornual sinus	Is a	False	Skin part	Inferred relationship	Some
Epidermis structure	Is a	True	Skin part	Inferred relationship	Some
Ischial callosity	Is a	False	Skin part	Inferred relationship	Some
Feather shaft	Is a	False	Skin part	Inferred relationship	Some
Feather follicle	Is a	False	Skin part	Inferred relationship	Some
Skin appendage structure (body structure)	Is a	False	Skin part	Inferred relationship	Some
Abdominal skin pouch structure	Is a	False	Skin part	Inferred relationship	Some
Surface feature of skin	Is a	False	Skin part	Inferred relationship	Some
Skin structure under microscope (body structure)	Is a	True	Skin part	Inferred relationship	Some
Mucocutaneous junction	Is a	False	Skin part	Inferred relationship	Some
Structure of cleavage lines of skin	Is a	True	Skin part	Inferred relationship	Some
Structure of dermatoglyphic patterns	Is a	True	Skin part	Inferred relationship	Some
Structure of tension lines of skin	Is a	True	Skin part	Inferred relationship	Some
Aplasia cutis congenita (disorder)	Finding site	True	Skin part	Inferred relationship	Some	1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder)	Finding site	True	Skin part	Inferred relationship	Some	1
Aplasia cutis congenita due to teratogenic drug (Type 7) (disorder)	Finding site	True	Skin part	Inferred relationship	Some	1
Aplasia cutis congenita associated with fetus papyraceus (Type 5) (disorder)	Finding site	True	Skin part	Inferred relationship	Some	1
Aplasia cutis in Johanson-Blizzard syndrome (disorder)	Finding site	True	Skin part	Inferred relationship	Some	1
Aplasia cutis congenita due to underlying malformation (Type 4) (disorder)	Finding site	True	Skin part	Inferred relationship	Some	1
Adams-Oliver syndrome	Finding site	False	Skin part	Inferred relationship	Some	2
Congenital absence of skin on scalp with epidermal naevi	Finding site	False	Skin part	Inferred relationship	Some	1
Aplasia cutis congenita following intra-uterine infection (Type 8) (disorder)	Finding site	True	Skin part	Inferred relationship	Some	1
Aplasia cutis in Trisomy 13 syndrome (disorder)	Finding site	True	Skin part	Inferred relationship	Some	1
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn) (disorder)	Finding site	True	Skin part	Inferred relationship	Some	1
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) (disorder)	Finding site	True	Skin part	Inferred relationship	Some	1
Oculocerebrocutaneous syndrome (disorder)	Finding site	True	Skin part	Inferred relationship	Some	1
A rare disorder characterized by the association of aplasia cutis congenita with high myopia, congenital nystagmus and cone-rod dysfunction. It has been described in two siblings (brother and sister). Transmission is autosomal dominant.	Finding site	False	Skin part	Inferred relationship	Some	2
An extremely rare association syndrome, described in only two brothers to date (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to intestinal lymphangiectasia. There have been no further descriptions in the literature since 1985.	Finding site	True	Skin part	Inferred relationship	Some	2
A rare ectodermal dysplasia characterized by the association of epibulbar dermoids and aplasia cutis congenital.	Finding site	True	Skin part	Inferred relationship	Some	2
Blood vessel structure of skin (body structure)	Is a	True	Skin part	Inferred relationship	Some
A rare disorder characterized by the association of aplasia cutis congenita with high myopia, congenital nystagmus and cone-rod dysfunction. It has been described in two siblings (brother and sister). Transmission is autosomal dominant.	Finding site	True	Skin part	Inferred relationship	Some	1
SCALP syndrome is a rare skin disease characterized by the association of sebaceous nevus and aplasia cutis congenita (usually on the scalp and face) in conjunction with limbal dermoid of the eye, a giant congenital melanocytic nevus and variable central nervous system abnormalities, including seizures, hydrocephalus, neurocutaneous melanosis, arachnoid cysts, and diffuse unilateral hemisphere enlargement.	Finding site	True	Skin part	Inferred relationship	Some	2
A rare skin disorder characterized by the co-occurrence of sebaceous nevi with aplasia cutis congenita located directly adjacent or in close proximity and ocular abnormalities including limbal dermoids and coloboma of the conjunctiva.	Finding site	True	Skin part	Inferred relationship	Some	1
Congenital absence of skin on scalp	Finding site	True	Skin part	Inferred relationship	Some	2
Aplasia cutis congenita of limb (disorder)	Finding site	True	Skin part	Inferred relationship	Some	2
Autosomal recessive aplasia cutis congenita of limb (disorder)	Finding site	True	Skin part	Inferred relationship	Some	2
Partial bed bath	Procedure site - Direct (attribute)	True	Skin part	Inferred relationship	Some	1
Structure of lymphatic vessel of skin (body structure)	Is a	True	Skin part	Inferred relationship	Some

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
452148019	Skin part	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
705299011	Skin part (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core