oculocerebral hypopigmentation syndrome type preus

Preferred Label : oculocerebral hypopigmentation syndrome type preus;

MeSH synonym : Oculocerebral Hypopigmentation Syndrome of Preus;

Related MeSH term : Cross syndrome; Kramer Syndrome; Oculocerebral syndrome with hypopigmentation;

Details

Origin ID

C537866;

UMLS CUI

C2931646;

Automatic exact mappings (from CISMeF team)
- Cross syndrome (disorder) [SNOMED CT concept]
- Oculocerebral hypopigmentation syndrome, Cross type [ORDO Disease]
- Oculocerebral syndrome with hypopigmentation [ICD-11 More detail]
- cross syndrome [SNOMED Notion]
Currated CISMeF NLP mapping
- Oculocerebral hypopigmentation syndrome of Preus type (disorder) [SNOMED CT concept]
- Oculocerebral hypopigmentation syndrome of preus [OMIM Phenotype]
- Oculocerebral hypopigmentation syndrome, Preus type [ORDO Disease]
MeSH term(s) associated for indexing
- abnormalities, multiple [MeSH Descriptor]
- craniofacial abnormalities [MeSH Descriptor]
- pigmentation disorders [MeSH Descriptor]
ORDO relation(s)
- Oculocerebral hypopigmentation syndrome, Preus type [ORDO Disease]
Record concept(s)
- Cross syndrome [MeSH concept]
- Oculocerebral hypopigmentation syndrome type Preus [MeSH concept]
See also inter- (CISMeF)
- Oculocerebral hypopigmentation syndrome, Cross type [ORDO Disease]
- Oculocerebral syndrome with hypopigmentation [OMIM Phenotype]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Oculocerebral hypopigmentation syndrome of Preus type (disorder) [SNOMED CT concept]
- Oculocerebral hypopigmentation syndrome of preus [OMIM Phenotype]
- Oculocerebral hypopigmentation syndrome, Preus type [ORDO Disease]
Validated automatic mappings to NTBT
- Albinism [ICD-10 Sub-category (who)]
- Albinism [ICD-10 Sub-category]

Keyword's position in hierarchy(ies) :

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