hypopigmentation-immunodeficiency disease

Preferred Label : hypopigmentation-immunodeficiency disease;

Origin ID

D6-A2620;

UMLS CUI

C0398794;

Currated CISMeF NLP mapping
- Griscelli syndrome [ORDO Disease]
- Griscelli syndrome [MedDRA Preferred Term]
- Hypopigmentation-immunodeficiency disease (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Albinism [ICD-10 Sub-category (who)]
Metaterm(s)
- metabolism [CISMeF Metaterm]
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Hypopigmentation-immunodeficiency disease (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Griscelli syndrome [ORDO Disease]
- Griscelli syndrome [Disease (Nov.)]
- Griscelli syndrome [DO Concept]
- Griscelli syndrome [MedDRA Preferred Term]
- Hypopigmentation-immunodeficiency disease (disorder) [SNOMED CT concept]