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18822004: Centrofacial lentiginosis syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
31738018 Centrofacial lentiginosis syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
746397018 Centrofacial lentiginosis syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1222190018 Centrofacial lentiginosis en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Centrofacial lentiginosis syndrome Is a Congenital anomaly of integument false Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Is a Congenital hamartosis false Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Is a Lentigo false Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Pathological process Benign neoplastic process false Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 3
Centrofacial lentiginosis syndrome Associated morphology Pigmented nevus, no International Classification of Diseases for Oncology subtype false Inferred relationship Existential restriction modifier 2
Centrofacial lentiginosis syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Centrofacial lentiginosis syndrome Associated morphology Hyperpigmentation false Inferred relationship Existential restriction modifier 1
Centrofacial lentiginosis syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Centrofacial lentiginosis syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Centrofacial lentiginosis syndrome Is a Lentigo false Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Is a Site-specific disorder of skin false Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Is a Lentiginosis true Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Centrofacial lentiginosis syndrome Associated morphology Increased melanin pigmentation false Inferred relationship Existential restriction modifier 1
Centrofacial lentiginosis syndrome Associated morphology Increased melanin pigmentation false Inferred relationship Existential restriction modifier 1
Centrofacial lentiginosis syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Centrofacial lentiginosis syndrome Is a Congenital hamartoma false Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Centrofacial lentiginosis syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier 2
Centrofacial lentiginosis syndrome Finding site Skin structure of face true Inferred relationship Existential restriction modifier 1
Centrofacial lentiginosis syndrome Is a Congenital hamartoma of skin true Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Associated morphology Lentigo true Inferred relationship Existential restriction modifier 1
Centrofacial lentiginosis syndrome Is a Congenital anomaly of face false Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Is a Mass of head false Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Is a Genetic disorder of skin pigmentation false Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Is a Congenital pigmentary skin anomalies false Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Centrofacial lentiginosis syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Is a Lesion of skin of face true Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Is a Congenital melanosis true Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
Centrofacial lentiginosis syndrome Is a Mass of skin of head true Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Is a Hereditary hypermelanosis true Inferred relationship Existential restriction modifier
Centrofacial lentiginosis syndrome Is a Developmental hereditary disorder false Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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