89031001: hypopigmentatie (afwijkende morfologie)

SNOMED CT Concept\Body structure\Morphologically altered structure\Morphologically abnormal structure (morphologic abnormality)\Lesion (morphologic abnormality)\Pigment alteration\Hypopigmentation

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hypopigmentation	Is a	Pigment alteration	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Woolf's syndrome	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Deafness, vitiligo, achalasia syndrome	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	3
Brown oculocutaneous albinism	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	2
Brown oculocutaneous albinism	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Microcephalus with albinism and digital anomaly syndrome (disorder)	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	5
Microcephalus with albinism and digital anomaly syndrome (disorder)	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	4
Oculocutaneous albinism type 5 (disorder)	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Oculocutaneous albinism type 5 (disorder)	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	2
Deaf blind hypopigmentation syndrome Yemenite type (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	2
Oculocutaneous albinism	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	2
Oculocutaneous albinism	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Congenital hypopigmentation of choroid	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Oculocerebral hypopigmentation syndrome of Preus type (disorder)	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	2
Oculocerebral hypopigmentation syndrome of Preus type (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Minimal pigment oculocutaneous albinism	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	2
Minimal pigment oculocutaneous albinism	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Temperature-sensitive oculocutaneous albinism	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	2
Temperature-sensitive oculocutaneous albinism	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Albinism	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
oculocutaan albinisme met congenitaal perceptief gehoorverlies	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	2
Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	5
Chédiak-Higashi syndrome	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Oculocutaneous albinoidism	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Tyrosinase-negative oculocutaneous albinism	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Tyrosinase-negative oculocutaneous albinism	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	2
Hermansky-Pudlak syndrome	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	2
Hermansky-Pudlak syndrome	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Albinism co-occurrent with hematologic disorder (disorder)	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Albinism with deafness syndrome (disorder)	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Yellow mutant oculocutaneous albinism	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	2
Yellow mutant oculocutaneous albinism	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Piebald trait with neurologic defects syndrome	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Attenuated Chédiak-Higashi syndrome (disorder)	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	2
Congenital deficiency of pigment of skin	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
parodontitis gelijktijdig met syndroom van Chédiak-Higashi (aandoening)	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	2
Oculocutaneous albinism type 6 (disorder)	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Oculocutaneous albinism type 6 (disorder)	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	2
Albinotic fundus	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Partial albinism	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Congenital oculocutaneous hypopigmentation	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Congenital oculocutaneous hypopigmentation	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	2
Tyrosinase-positive oculocutaneous albinism	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Tyrosinase-positive oculocutaneous albinism	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	2
Punctate oculocutaneous albinoidism	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Waardenburg syndrome	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Albinism-deafness syndrome of Tietz (disorder)	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Vitiligo of pinta	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Vitiligo of skin of left eyelid and periocular area (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Vitiligo of skin of left upper eyelid and periocular area (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Vitiligo of skin of right upper eyelid and periocular area (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Vitiligo of skin of right eyelid and periocular area (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Waardenburg syndrome type 3	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1
Waardenburg syndrome type 1 (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Waardenburg syndrome type 2 (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Confetti-like atrophic macular lesions of skin (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	2
Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	5
Laser-induced hypopigmentation (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Hypopigmentation of left eyelid and periocular area	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Hypopigmentation of right eyelid and periocular area (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Hypopigmentation of left lower eyelid and periocular area	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Hypopigmentation of right lower eyelid and periocular area (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Vitiligo of skin of upper eyelid (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	2
Vitiligo of skin of lower eyelid (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	2
Progressive macular hypomelanosis	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Waardenburg syndrome type 3 (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	2
Waardenburg syndrome type 1 (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	5
Waardenburg syndrome type 2 (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	2
Vitiligo of mucous membrane (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	1
Vitiligo of mucous membrane (disorder)	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	2
Nongeographic atrophy of macula	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	3
Cutis tricolor	Associated morphology	True	Hypopigmentation	Inferred relationship	Some	2
progressieve maculaire hypomelanose (aandoening)	Associated morphology	False	Hypopigmentation	Inferred relationship	Some	1

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Reference Sets

Dutch pathology simple reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
147619012	Hypopigmentation	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
831840012	Hypopigmentation (morphologic abnormality)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
918231000146114	hypopigmentatie (afwijkende morfologie)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
918241000146118	hypopigmentatie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
9405421000146112	Afname van pigment in de huid, waardoor witte vlekken ontstaan.	nl	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)