111306001: Multiple lentigines syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin or mucosa lesion\Lentiginosis\Multiple lentigines syndrome
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Multiple lentigines syndrome

\Mass of body structure\Lentiginosis\Multiple lentigines syndrome

\General finding of soft tissue\Skin finding\Disorder of skin\Congenital anomaly of skin\Multiple lentigines syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Multiple lentigines syndrome

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Multiple lentigines syndrome
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Multiple lentigines syndrome
\Integumentary system finding\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Multiple lentigines syndrome
\Integumentary system finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Multiple lentigines syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Multiple lentigines syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Multiple lentigines syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Multiple lentigines syndrome
\Disease\Disorder of pigmentation\Melanosis\Lentiginosis\Multiple lentigines syndrome
\Disease\Neoplasm and/or hamartoma\Hamartoma\Lentiginosis\Multiple lentigines syndrome
\Disease\Degenerative disorder\Melanosis\Lentiginosis\Multiple lentigines syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Multiple lentigines syndrome
\Disease\Disorder of body system\Skin or mucosa lesion\Lentiginosis\Multiple lentigines syndrome
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Multiple lentigines syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Multiple lentigines syndrome
\Disease\Disorder of body system\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Multiple lentigines syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin\Multiple lentigines syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Multiple lentigines syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\Multiple lentigines syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin\Multiple lentigines syndrome

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

178538018 Multiple lentigines syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
187732010 LEOPARD syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
630152013 Multiple lentigines syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1215882014 Generalised lentiginosis en Synonym Inactive Only initial character case insensitive SNOMED CT core module
1217385016 Generalized lentiginosis en Synonym Inactive Only initial character case insensitive SNOMED CT core module
1219626017 Leopard syndrome lentiginosis en Synonym Active Entire term case insensitive SNOMED CT core module
1219627014 Leopard syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Multiple lentigines syndrome	Is a	Congenital hamartosis	false	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Is a	Lentigo	false	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Is a	Congenital anomaly of skin	true	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Associated morphology	Pigmented nevus, no International Classification of Diseases for Oncology subtype	false	Inferred relationship	Existential restriction modifier	1
Multiple lentigines syndrome	Pathological process	Benign neoplastic process	false	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	3
Multiple lentigines syndrome	Finding site	Structure of skin region	false	Inferred relationship	Existential restriction modifier	1
Multiple lentigines syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Associated morphology	Hyperpigmentation	false	Inferred relationship	Existential restriction modifier	2
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Multiple lentigines syndrome	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Multiple lentigines syndrome	Is a	Benign neoplasm of skin	false	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Finding site	Structure of skin region	false	Inferred relationship	Existential restriction modifier	1
Multiple lentigines syndrome	Is a	Lentigo	false	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Is a	Acquired melanocytic nevus	false	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Is a	Melanocytic nevus of skin	false	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Is a	Melanocytic tumor of skin	false	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Associated morphology	Hamartoma	false	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	3
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Multiple lentigines syndrome	Is a	Neoplasm of skin region	false	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Associated morphology	Structure showing abnormal deposition of pigment	false	Inferred relationship	Existential restriction modifier	3
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	3
Multiple lentigines syndrome	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Is a	Hereditary disorder of the integument	true	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Associated morphology	Increased melanin pigmentation	false	Inferred relationship	Existential restriction modifier	2
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Multiple lentigines syndrome	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier	1
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Multiple lentigines syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	3
Multiple lentigines syndrome	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	3
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	3
Multiple lentigines syndrome	Is a	Genetic disorder of skin pigmentation	false	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Is a	Lentiginosis	true	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Associated morphology	Lentigo	true	Inferred relationship	Existential restriction modifier	2
Multiple lentigines syndrome	Is a	Mass of soft tissue	false	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Finding site	Skin and/or subcutaneous tissue structure	false	Inferred relationship	Existential restriction modifier	1
Multiple lentigines syndrome	Is a	Soft tissue lesion	false	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Finding site	Structure of skin and/or mucous membrane	true	Inferred relationship	Existential restriction modifier	2
Multiple lentigines syndrome	Is a	Hamartoma of integument	false	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Is a	Mass of body region	false	Inferred relationship	Existential restriction modifier
Multiple lentigines syndrome	Associated morphology	Lentigo	false	Inferred relationship	Existential restriction modifier	1
Multiple lentigines syndrome	Pathological process	Pathological developmental process	false	Inferred relationship	Existential restriction modifier	3
Multiple lentigines syndrome	Finding site	Skin and/or subcutaneous tissue structure	false	Inferred relationship	Existential restriction modifier	3
Multiple lentigines syndrome	Associated morphology	Lentigo	false	Inferred relationship	Existential restriction modifier	3
Multiple lentigines syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	1
Multiple lentigines syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Multiple lentigines syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Multiple lentigines syndrome	Pathological process	Pathological developmental process	false	Inferred relationship	Existential restriction modifier	2
Multiple lentigines syndrome	Is a	Developmental hereditary disorder	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
178538018	Multiple lentigines syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
187732010	LEOPARD syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
630152013	Multiple lentigines syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
1215882014	Generalised lentiginosis	en	Synonym	Inactive	Only initial character case insensitive	SNOMED CT core module
1217385016	Generalized lentiginosis	en	Synonym	Inactive	Only initial character case insensitive	SNOMED CT core module
1219626017	Leopard syndrome lentiginosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1219627014	Leopard syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module