FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

37257004: Decreased melanin pigmentation (morphologic abnormality)

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
62162011 Decreased melanin pigmentation en Synonym Active Entire term case insensitive SNOMED CT core module
769103011 Decreased melanin pigmentation (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Decreased melanin pigmentation Is a Hypopigmentation true Inferred relationship Existential restriction modifier
Decreased melanin pigmentation Is a Abnormal melanin pigmentation true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Tyrosinase-negative oculocutaneous albinism Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 3
Temperature-sensitive oculocutaneous albinism Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 3
Cross syndrome Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 5
Chédiak-Higashi syndrome Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 3
Phylloid hypomelanosis Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Black locks, oculocutaneous albinism, AND deafness of the sensorineural type Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Punctate oculocutaneous albinoidism Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Oculocutaneous albinoidism Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Aland eye disease and ocular albinism Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Ocular albinism Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Ocular albinism, type I Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Autosomal recessive ocular albinism Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Hypopigmentation-immunodeficiency disease Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Partial albinism Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 1
Albinism-deafness syndrome of Tietz Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 1
Ocular albinism-lentigines-deafness syndrome Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 4
Albinism Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 1
Ziprkowski-Margolis syndrome Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 1
Woolf's syndrome Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 1
Phylloid hypomelanosis Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 1
Black locks, oculocutaneous albinism, AND deafness of the sensorineural type Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 3
Brown oculocutaneous albinism Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Rufous albinism Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Hermansky-Pudlak syndrome Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Tyrosinase-positive oculocutaneous albinism Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Minimal pigment oculocutaneous albinism Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Yellow mutant oculocutaneous albinism Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Tyrosinase-negative oculocutaneous albinism Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Temperature-sensitive oculocutaneous albinism Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Periodontitis co-occurrent with Chédiak-Higashi syndrome Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 6
Arsenic-induced rain-drop hypomelanosis Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Albinism co-occurrent with hematologic disorder Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 3
Oculocutaneous albinism type 4 Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 4
Oculocutaneous albinism type 4 Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 5
Microcephalus with albinism and digital anomaly syndrome Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 10
Microcephalus with albinism and digital anomaly syndrome Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 8
Attenuated Chédiak-Higashi syndrome Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 4
Attenuated Chédiak-Higashi syndrome Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 5
Ocular albinism with late-onset sensorineural deafness Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 6
Ocular albinism with late-onset sensorineural deafness Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 8
Oculocutaneous albinism type 5 Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 4
Oculocutaneous albinism type 6 Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 4
Oculocutaneous albinism type 7 Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 4
Oculocutaneous albinism type 5 Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 5
Oculocutaneous albinism type 6 Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 5
Oculocutaneous albinism type 7 Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 5
Albinism with deafness syndrome Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 7
Oculocutaneous albinism type 1 Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 3
Syphilitic leukoderma Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Ocular albinism with late-onset sensorineural deafness Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 1
Ocular albinism with congenital sensorineural deafness Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 3
Oculocutaneous albinism type 5 Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism type 5 Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 1
Cross syndrome Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 4
Oculocutaneous albinism type 6 Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism type 6 Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism type 7 Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism type 7 Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 1
Microcephalus with albinism and digital anomaly syndrome Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 5
Microcephalus with albinism and digital anomaly syndrome Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 4
Punctate oculocutaneous albinoidism Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism type 4 Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism type 4 Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism type 1 Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism type 1 Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 1
Periodontitis co-occurrent with Chédiak-Higashi syndrome Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 4
Hypopigmentation-immunodeficiency disease Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 3
Albinism co-occurrent with hematologic disorder Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 2
Albinism with deafness syndrome Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 4
Hypomelanotic sarcoidosis Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 3
Hypopigmentation-immunodeficiency disease type 1 Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 1
Hypopigmentation-immunodeficiency disease type 3 Associated morphology True Decreased melanin pigmentation Inferred relationship Existential restriction modifier 1
Leukoderma NOS (disorder) Associated morphology False Decreased melanin pigmentation Inferred relationship Existential restriction modifier 1

Start Page 2 of 2

This concept is not in any reference sets

Back to Start