Oslam syndrome

Preferred Label : Oslam syndrome;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Osteosarcoma, limb anomalies, and macrocytosis; Osteosarcoma, limb anomalies, and erythroid macrocytosis with megaloblastic marrow;

Inheritance : Autosomal dominant;

Prefixed ID : %165660;

Détails

Origin ID

165660;

UMLS CUI

C1833792;

Currated CISMeF NLP mapping
- OSLAM syndrome [ORDO Disease]
- Oslam syndrome [MeSH concept]
- Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome (disorder) [SNOMED CT concept]
- oslam syndrome [MeSH Supplementary Concept]
HPO term(s)
- Anemia [HPO term]
- Autosomal dominant inheritance [HPO term]
- Clinodactyly [HPO term]
- Neoplasm [HPO term]
- Osteosarcoma [HPO term]
- Radial deviation of finger [HPO term]
- Radioulnar synostosis [HPO term]
ORDO concept(s)
- OSLAM syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- OSLAM syndrome [ORDO Disease]
- Oslam syndrome [MeSH concept]
- Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome (disorder) [SNOMED CT concept]
- oslam syndrome [MeSH Supplementary Concept]

Position du mot-clé dans l'(les) arborescence(s) :

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