Blue rubber bleb nevus

Preferred Label : Blue rubber bleb nevus;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Bean syndrome;

Inheritance : Autosomal dominant;

Prefixed ID : %112200;

Details

Origin ID

112200;

UMLS CUI

C0346072;

Currated CISMeF NLP mapping
- Blue Rubber Bleb Nevus [NCIt concept]
- Blue rubber bleb naevus syndrome [ICD-11 More detail]
- Blue rubber bleb nevus [ORDO Disease]
- Blue rubber bleb nevus (disorder) [SNOMED CT concept]
- Blue rubber bleb nevus syndrome [MeSH concept]
- blue rubber bleb nevus syndrome [Disease (Nov.)]
- blue rubber bleb nevus syndrome [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the liver [HPO term]
- Abnormality of the mouth [HPO term]
- Abnormality of the respiratory system [HPO term]
- Autosomal dominant inheritance [HPO term]
- Cerebellar medulloblastoma [HPO term]
- Chronic disseminated intravascular coagulation [HPO term]
- Hemangioma [HPO term]
- Hypermelanotic macule [HPO term]
- Intestinal bleeding [HPO term]
- Intussusception [HPO term]
- Iron deficiency anemia [HPO term]
- Pathologic fracture [HPO term]
- Rectal prolapse [HPO term]
- Thrombocytopenia [HPO term]
- Volvulus [HPO term]
- macules [HPO term]
ORDO concept(s)
- Blue rubber bleb nevus [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Blue Rubber Bleb Nevus [NCIt concept]
- Blue rubber bleb nevus [ORDO Disease]
- Blue rubber bleb nevus (disorder) [SNOMED CT concept]
- Blue rubber bleb nevus syndrome [MeSH concept]
- blue rubber bleb nevus syndrome [MeSH Supplementary Concept]
- blue rubber bleb nevus syndrome [Disease (Nov.)]

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