403807001: Phylloid hypomelanosis (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\Phylloid hypomelanosis
\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\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Skin AND/OR mucosa finding\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Disorder of skin pigmentation\Hypopigmentation of skin\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Genetic disorder of skin pigmentation\Phylloid hypomelanosis
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Hypopigmentation of skin\Congenital deficiency of pigment of skin\Phylloid hypomelanosis

\General finding of soft tissue\Skin finding\Disorder of skin\Congenital anomaly of skin\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\General finding of soft tissue\Skin finding\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Genetic disorder of skin pigmentation\Phylloid hypomelanosis
\General finding of soft tissue\Skin finding\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\General finding of soft tissue\Skin finding\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Hypopigmentation of skin\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\General finding of soft tissue\Disorder of soft tissue\Soft tissue lesion\Skin lesion\Disorder of skin pigmentation\Genetic disorder of skin pigmentation\Phylloid hypomelanosis
\General finding of soft tissue\Disorder of soft tissue\Soft tissue lesion\Skin lesion\Disorder of skin pigmentation\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\General finding of soft tissue\Disorder of soft tissue\Soft tissue lesion\Skin lesion\Disorder of skin pigmentation\Hypopigmentation of skin\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Genetic disorder of skin pigmentation\Phylloid hypomelanosis
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Hypopigmentation of skin\Congenital deficiency of pigment of skin\Phylloid hypomelanosis

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Phylloid hypomelanosis
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Genetic disorder of skin pigmentation\Phylloid hypomelanosis
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Hypopigmentation of skin\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Integumentary system finding\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Integumentary system finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Integumentary system finding\Skin finding\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Genetic disorder of skin pigmentation\Phylloid hypomelanosis
\Integumentary system finding\Skin finding\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Integumentary system finding\Skin finding\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Hypopigmentation of skin\Congenital deficiency of pigment of skin\Phylloid hypomelanosis

\Disease\Genetic disease\Genetic disorder of skin pigmentation\Phylloid hypomelanosis
\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Albinism\Phylloid hypomelanosis
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Phylloid hypomelanosis
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Albinism\Phylloid hypomelanosis
\Disease\Disorder of pigmentation\Disorder of skin pigmentation\Genetic disorder of skin pigmentation\Phylloid hypomelanosis
\Disease\Disorder of pigmentation\Disorder of skin pigmentation\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Disease\Disorder of pigmentation\Disorder of skin pigmentation\Hypopigmentation of skin\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Disease\Disorder of pigmentation\Albinism\Phylloid hypomelanosis
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Phylloid hypomelanosis
\Disease\Disorder of body system\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Disorder of skin pigmentation\Genetic disorder of skin pigmentation\Phylloid hypomelanosis
\Disease\Disorder of body system\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Disorder of skin pigmentation\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Disease\Disorder of body system\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Disorder of skin pigmentation\Hypopigmentation of skin\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Phylloid hypomelanosis
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Genetic disorder of skin pigmentation\Phylloid hypomelanosis
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Hypopigmentation of skin\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Disease\Disorder of body system\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Albinism\Phylloid hypomelanosis
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Disease\Congenital disease\Congenital malformation\Albinism\Phylloid hypomelanosis
\Disease\Congenital disease\Inborn error of metabolism\Albinism\Phylloid hypomelanosis
\Disease\Disorder of soft tissue\Soft tissue lesion\Skin lesion\Disorder of skin pigmentation\Genetic disorder of skin pigmentation\Phylloid hypomelanosis
\Disease\Disorder of soft tissue\Soft tissue lesion\Skin lesion\Disorder of skin pigmentation\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Disease\Disorder of soft tissue\Soft tissue lesion\Skin lesion\Disorder of skin pigmentation\Hypopigmentation of skin\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Genetic disorder of skin pigmentation\Phylloid hypomelanosis
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Disorder of skin pigmentation\Hypopigmentation of skin\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Disease\Developmental disorder\Developmental hereditary disorder\Albinism\Phylloid hypomelanosis
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin\Congenital pigmentary skin anomalies\Congenital deficiency of pigment of skin\Phylloid hypomelanosis
\Disease\Developmental disorder\Congenital malformation\Albinism\Phylloid hypomelanosis

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

1771733017 Phylloid hypomelanosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

1782816012 Phylloid hypomelanosis en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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