239089006: Acromelanosis (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Disorder of skin pigmentation\Genetic disorder of skin pigmentation\Hereditary hypermelanosis\Acromelanosis
\Skin AND/OR mucosa finding\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Disorder of skin pigmentation\Genetic disorder of skin pigmentation\Inherited cutaneous hyperpigmentation\Acromelanosis
\Skin AND/OR mucosa finding\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Disorder of skin pigmentation\Congenital pigmentary skin anomalies\Inherited cutaneous hyperpigmentation\Acromelanosis
\Skin AND/OR mucosa finding\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Disorder of skin pigmentation\Hyperpigmentation of skin\Hereditary hypermelanosis\Acromelanosis
\Skin AND/OR mucosa finding\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Disorder of skin pigmentation\Hyperpigmentation of skin\Inherited cutaneous hyperpigmentation\Acromelanosis
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Degenerative skin disorder\Skin deposits\Hyperpigmentation of skin\Hereditary hypermelanosis\Acromelanosis
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Degenerative skin disorder\Skin deposits\Hyperpigmentation of skin\Inherited cutaneous hyperpigmentation\Acromelanosis
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Inherited cutaneous hyperpigmentation\Acromelanosis
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Congenital pigmentary skin anomalies\Inherited cutaneous hyperpigmentation\Acromelanosis
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Genetic disorder of skin pigmentation\Hereditary hypermelanosis\Acromelanosis
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Genetic disorder of skin pigmentation\Inherited cutaneous hyperpigmentation\Acromelanosis
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Congenital pigmentary skin anomalies\Inherited cutaneous hyperpigmentation\Acromelanosis
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Hyperpigmentation of skin\Hereditary hypermelanosis\Acromelanosis
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Hyperpigmentation of skin\Inherited cutaneous hyperpigmentation\Acromelanosis

\Finding of limb structure\Disorder of extremity\...

\Disorder of digit\Congenital anomaly of digit\Acromelanosis

\Congenital anomaly of limb\Congenital anomaly of digit\Acromelanosis

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

358306014 Acromelanosis en Synonym Active Entire term case insensitive SNOMED CT core module

628058019 Acromelanosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Acromelanosis	Is a	Inherited cutaneous hyperpigmentation	true	Inferred relationship	Existential restriction modifier
Acromelanosis	Associated morphology	Hyperpigmentation	false	Inferred relationship	Existential restriction modifier	3
Acromelanosis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Acromelanosis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Acromelanosis	Finding site	Structure of skin region	false	Inferred relationship	Existential restriction modifier	3
Acromelanosis	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	2
Acromelanosis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Acromelanosis	Associated morphology	Melanosis	true	Inferred relationship	Existential restriction modifier	1
Acromelanosis	Finding site	Skin structure of digit	true	Inferred relationship	Existential restriction modifier	1
Acromelanosis	Is a	Melanosis	false	Inferred relationship	Existential restriction modifier
Acromelanosis	Is a	Disorder of digit	false	Inferred relationship	Existential restriction modifier
Acromelanosis	Is a	Disorder of soft tissue of limb	false	Inferred relationship	Existential restriction modifier
Acromelanosis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Acromelanosis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	3
Acromelanosis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Acromelanosis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	3
Acromelanosis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Acromelanosis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	3
Acromelanosis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Acromelanosis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	3
Acromelanosis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	4
Acromelanosis	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	4
Acromelanosis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	4
Acromelanosis	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Acromelanosis	Is a	Congenital anomaly of digit	true	Inferred relationship	Existential restriction modifier
Acromelanosis	Is a	Congenital melanosis	true	Inferred relationship	Existential restriction modifier
Acromelanosis	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Acromelanosis	Is a	Hereditary hypermelanosis	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
358306014	Acromelanosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
628058019	Acromelanosis (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module