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254158000: Autosomal dominant ichthyosis vulgaris (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
378338015 Autosomal dominant ichthyosis vulgaris en Synonym Active Entire term case insensitive SNOMED CT core module
378339011 ADI - Autosomal dominant ichthyosis vulgaris en Synonym Active Entire term case sensitive SNOMED CT core module
645010017 Autosomal dominant ichthyosis vulgaris (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant ichthyosis vulgaris Is a Ichthyosis vulgaris true Inferred relationship Existential restriction modifier
Autosomal dominant ichthyosis vulgaris Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Autosomal dominant ichthyosis vulgaris Occurrence Congenital false Inferred relationship Existential restriction modifier
Autosomal dominant ichthyosis vulgaris Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier
Autosomal dominant ichthyosis vulgaris Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Autosomal dominant ichthyosis vulgaris Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Autosomal dominant ichthyosis vulgaris Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Autosomal dominant ichthyosis vulgaris Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Autosomal dominant ichthyosis vulgaris Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Autosomal dominant ichthyosis vulgaris Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Autosomal dominant ichthyosis vulgaris Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Autosomal dominant ichthyosis vulgaris Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Autosomal dominant ichthyosis vulgaris Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Autosomal dominant ichthyosis vulgaris Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 1
Autosomal dominant ichthyosis vulgaris Is a Autosomal dominant ichthyosis true Inferred relationship Existential restriction modifier
Autosomal dominant ichthyosis vulgaris Associated morphology Follicular hyperkeratosis false Inferred relationship Existential restriction modifier 1
Autosomal dominant ichthyosis vulgaris Has interpretation Abnormal true Inferred relationship Existential restriction modifier 2
Autosomal dominant ichthyosis vulgaris Finding site Hair follicle structure false Inferred relationship Existential restriction modifier 1
Autosomal dominant ichthyosis vulgaris Interprets Keratinization, function true Inferred relationship Existential restriction modifier 2
Autosomal dominant ichthyosis vulgaris Finding site Entire skin true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Ichthyosis cheek eyebrow syndrome Is a False Autosomal dominant ichthyosis vulgaris Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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