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721904001: Rombo syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3326812012 Rombo syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3326813019 Rombo syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Rombo syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Rombo syndrome Is a Hypotrichosis true Inferred relationship Existential restriction modifier
Rombo syndrome Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Rombo syndrome Is a Atrophoderma false Inferred relationship Existential restriction modifier
Rombo syndrome Is a Hereditary cancer-predisposing syndrome true Inferred relationship Existential restriction modifier
Rombo syndrome Finding site Hair structure false Inferred relationship Existential restriction modifier
Rombo syndrome Associated morphology Atrophy true Inferred relationship Existential restriction modifier 2
Rombo syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 2
Rombo syndrome Associated morphology Growth alteration true Inferred relationship Existential restriction modifier 1
Rombo syndrome Finding site Hair structure true Inferred relationship Existential restriction modifier 1
Rombo syndrome Is a Atrophic condition of skin true 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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