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733203002: Non-androgenic hypertrichosis co-occurrent and due to genetic disease (disorder)


Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3473001019 Non-androgenic hypertrichosis co-occurrent and due to genetic disease (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3473002014 Non-androgenic hypertrichosis co-occurrent and due to genetic disease en Synonym Active Case insensitive SNOMED CT core
3473003016 Non-androgenic hypertrichosis with genetic disease en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Non-androgenic hypertrichosis co-occurrent and due to genetic disease Associated morphology Growth alteration true Inferred relationship Some 1
Non-androgenic hypertrichosis co-occurrent and due to genetic disease Finding site Hair structure true Inferred relationship Some 1
Non-androgenic hypertrichosis co-occurrent and due to genetic disease Due to Hereditary disease true Inferred relationship Some 2
Non-androgenic hypertrichosis co-occurrent and due to genetic disease Is a Hypertrichosis true Inferred relationship Some
Non-androgenic hypertrichosis co-occurrent and due to genetic disease Is a Hereditary disorder of the integument true Inferred relationship Some
Non-androgenic hypertrichosis co-occurrent and due to genetic disease Finding site Skin structure false Inferred relationship Some
Non-androgenic hypertrichosis co-occurrent and due to genetic disease Finding site Hair structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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