Cerebral cavernous malformations 3

Preferred Label : Cerebral cavernous malformations 3;

Symbol : CCM3;

CISMeF acronym : CCM3;

Type : Phenotype, molecular basis known;

Prefixed ID : #603285;

Details

Origin ID

603285;

UMLS CUI

C1864040;

Broader ORDO disease(s)
- Cerebral cavernous malformations [ORDO Disease]
CISMeF manual mappings
- cerebral cavernous malformation type 3 [Disease (Nov.)]
Currated CISMeF NLP mapping
- cerebral cavernous malformation 3 [DO Concept]
- cerebral cavernous malformations 3 [MeSH concept]
- cerebral cavernous malformations 3 [MeSH Supplementary Concept]
DO Cross reference
- cerebral cavernous malformation 3 [DO Concept]
Genes related to phenotype
- Programmed cell death 10 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Cerebral cavernous malformation [HPO term]
- Cerebral hemorrhage [HPO term]
- Headache [HPO term]
- Juvenile onset [HPO term]
- Paralysis [HPO term]
- Seizure [HPO term]
ORDO concept(s)
- Familial cerebral cavernous malformation [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- cerebral cavernous malformation 3 [DO Concept]
- cerebral cavernous malformation type 3 [Disease (Nov.)]
- cerebral cavernous malformations 3 [MeSH Supplementary Concept]
- cerebral cavernous malformations 3 [MeSH concept]

Keyword's position in hierarchy(ies) :

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