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403807001: Phylloid hypomelanosis (disorder)


Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1771733017 Phylloid hypomelanosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
1782816012 Phylloid hypomelanosis en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Phylloid hypomelanosis Pathological process Pathological developmental process true Inferred relationship Some 1
Phylloid hypomelanosis Associated morphology Hypopigmentation false Inferred relationship Some 1
Phylloid hypomelanosis Is a Congenital deficiency of pigment of skin true Inferred relationship Some
Phylloid hypomelanosis Is a Genetic disorder of skin pigmentation true Inferred relationship Some
Phylloid hypomelanosis Finding site Skin structure true Inferred relationship Some 1
Phylloid hypomelanosis Is a Hereditary disorder of the integument true Inferred relationship Some
Phylloid hypomelanosis Is a Albinism true Inferred relationship Some
Phylloid hypomelanosis Finding site Structure of skin region false Inferred relationship Some 1
Phylloid hypomelanosis Associated morphology Congenital hypopigmentation false Inferred relationship Some
Phylloid hypomelanosis Associated morphology Congenital deficiency false Inferred relationship Some
Phylloid hypomelanosis Occurrence Congenital false Inferred relationship Some
Phylloid hypomelanosis Finding site Eye region structure false Inferred relationship Some
Phylloid hypomelanosis Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Phylloid hypomelanosis Finding site Eye structure false Inferred relationship Some 2
Phylloid hypomelanosis Associated morphology Decreased melanin pigmentation false Inferred relationship Some
Phylloid hypomelanosis Occurrence Congenital true Inferred relationship Some 1
Phylloid hypomelanosis Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Phylloid hypomelanosis Occurrence Congenital false Inferred relationship Some 2
Phylloid hypomelanosis Associated morphology Decreased melanin pigmentation false Inferred relationship Some 2
Phylloid hypomelanosis Associated morphology Decreased melanin pigmentation true Inferred relationship Some 1

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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