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35484002: Aplasia cutis congenita (disorder)

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
59201011 Aplasia cutis congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
59202016 Epitheliogenesis imperfecta en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
59203014 Cutis aplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
767128014 Aplasia cutis congenita (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1228288018 Congenital absence of skin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1228289014 ACC - Aplasia cutis congenita en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
59201011 Aplasia cutis congenita en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
59201011 Aplasia cutis congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
59202016 Epitheliogenesis imperfecta en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
59202016 Epitheliogenesis imperfecta en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
59203014 Cutis aplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
59203014 Cutis aplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
767128014 Aplasia cutis congenita (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
767128014 Aplasia cutis congenita (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1228288018 Congenital absence of skin en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1228288018 Congenital absence of skin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1228289014 ACC - Aplasia cutis congenita en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1228289014 ACC - Aplasia cutis congenita en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3447531001000118 Aplasia cutis congenita de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
869321000172112 aplasia cutis congenita fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
869321000172112 aplasia cutis congenita fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3447531001000118 Aplasia cutis congenita de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

20 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Aplasia cutis congenita (disorder) Is a Skin lesion false Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis congenita (disorder) Is a Aplasia of skin true Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis congenita (disorder) Is a Nevi, hamartomas and developmental anomalies false Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis congenita (disorder) Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita (disorder) Finding site Structure of skin region (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis congenita (disorder) Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis congenita (disorder) Is a Site-specific disorder of skin false Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis congenita (disorder) Is a Congenital anomaly of skin (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis congenita (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita (disorder) Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Aplasia cutis congenita (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Aplasia cutis congenita (disorder) Is a Congenital absence false Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis congenita (disorder) Associated morphology Congenital partial absence false Inferred relationship Existential restriction modifier (core metadata concept) 2
Aplasia cutis congenita (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita (disorder) Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita (disorder) Finding site Skin part (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita (disorder) Associated morphology Aplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital absence of skin on scalp Is a True Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence of skin on scalp with epidermal nevi Is a True Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Adams-Oliver syndrome Is a True Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis congenita due to underlying malformation (Type 4) (disorder) Is a True Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis congenita associated with fetus papyraceus (Type 5) (disorder) Is a True Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) (disorder) Is a True Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis congenita due to teratogenic drug (Type 7) Is a True Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis congenita following intra-uterine infection (Type 8) Is a True Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Is a True Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis in Trisomy 13 syndrome Is a True Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn) (disorder) Is a True Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis in Johanson-Blizzard syndrome (disorder) Is a True Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis with myopia syndrome (disorder) Is a True Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis congenita with intestinal lymphangiectasia syndrome (disorder) Is a True Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare ectodermal dysplasia characterised by the association of epibulbar dermoids and aplasia cutis congenital. Is a True Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive aplasia cutis congenita of limb (disorder) Is a False Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare skin disease characterised by the association of sebaceous naevus and aplasia cutis congenita (usually on the scalp and face) in conjunction with limbal dermoid of the eye, a giant congenital melanocytic naevus and variable central nervous system abnormalities including seizures, hydrocephalus, neurocutaneous melanosis, arachnoid cysts, and diffuse unilateral hemisphere enlargement. Is a True Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Didymosis aplasticosebacea (disorder) Is a True Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis congenita of limb Is a True Aplasia cutis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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