Van den bosch syndrome

Preferred Label : Van den bosch syndrome;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : X-linked. ? contiguous gene syndrome;

Prefixed ID : %314500;

Details

Origin ID

314500;

UMLS CUI

C0796192;

Currated CISMeF NLP mapping
- Van den Bosch syndrome [ORDO Disease]
- Van den Bosch syndrome (disorder) [SNOMED CT concept]
- van den bosch syndrome [MeSH concept]
- van den bosch syndrome [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the skeletal system [HPO term]
- Acrokeratosis [HPO term]
- Anhidrosis [HPO term]
- Choroideremia [HPO term]
- Contiguous gene syndrome [HPO term]
- Intellectual disability [HPO term]
- X-linked inheritance [HPO term]
ORDO concept(s)
- Van den Bosch syndrome [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Van den Bosch syndrome [ORDO Disease]
- Van den Bosch syndrome (disorder) [SNOMED CT concept]
- van den bosch syndrome [MeSH Supplementary Concept]
- van den bosch syndrome [MeSH concept]

Keyword's position in hierarchy(ies) :

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