Familial progressive hyperpigmentation 715630006

SNOMED CT code

SNOMED code

715630006

name

Familial progressive hyperpigmentation

status

active

date introduced

2016-07-31

fully specified name(s)

Familial progressive hyperpigmentation (disorder)

synonyms

Familial progressive hyperpigmentation
Melanosis diffusa congenita
Melanosis universalis hereditaria
Universal melanosis

attributes - group1

Associated morphology

Melanosis 48010006

Finding site

Skin structure 39937001

parents

Autosomal dominant hereditary disorder 11164009
Hereditary hypermelanosis 403804008

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal dominant hereditary disorder 11164009
Familial progressive hyperpigmentation 715630006

SNOMED CT Concept 138875005
Clinical finding 404684003
Integumentary system finding 106077005
Disorder of integument 128598002
Hereditary disorder of the integument 363185004
Hereditary hypermelanosis 403804008
Familial progressive hyperpigmentation 715630006

ancestors

sorted most to least specific

Autosomal dominant hereditary disorder 11164009
Hereditary hypermelanosis 403804008
Autosomal hereditary disorder 1899006
Hereditary disorder of the integument 363185004
Melanosis 414662006
Hyperpigmentation of skin 49765009
Genetic disorder of skin pigmentation 724839001
Skin deposits 40449001
Disorder of skin pigmentation 46690002
Hereditary disorder by system 363137000
Hereditary disease 32895009
Degenerative skin disorder 396325007
Disorder of pigmentation 414032001
Skin lesion 95324001
Genetic disease 782964007
Degenerative disorder 362975008
Disorder of skin 95320005
Soft tissue lesion 239953001
Lesion of skin and/or skin-associated mucous membrane 714974000
Skin finding 106076001
Disorder of skin and/or subcutaneous tissue 80659006
Skin or mucosa lesion 247440002
Disorder of integument 128598002
Disorder of soft tissue 19660004
Skin AND/OR mucosa finding 415531008
Integumentary system finding 106077005
Disorder of body system 362965005
General finding of soft tissue 248402002
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Genetic disease 782964007

Hereditary disease 32895009

Autosomal hereditary disorder 1899006

Autosomal dominant hereditary disorder 11164009

Familial progressive hyperpigmentation 715630006

SNOMED CT code