Arteritis, familial granulomatous, with juvenile polyarthritis

Preferred Label : Arteritis, familial granulomatous, with juvenile polyarthritis;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Laboratory abnormalities : Elevated alkaline phosphatase;

Prefixed ID : 108050;

Détails

Origin ID

108050;

UMLS CUI

C1862510;

Currated CISMeF NLP mapping
- arteritis, familial granulomatous, with juvenile polyarthritis [MeSH concept]
- arteritis, familial granulomatous, with juvenile polyarthritis [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Elevated circulating alkaline phosphatase concentration [HPO term]
- Fever [HPO term]
- Granulomatous coronary arteritis [HPO term]
- Headache [HPO term]
- Hypertension [HPO term]
- Iritis [HPO term]
- Jaundice [HPO term]
- Papilledema [HPO term]
- Pericardial effusion [HPO term]
- Pleural effusion [HPO term]
- Rheumatoid arthritis [HPO term]
- Seizure [HPO term]
- Subcutaneous nodule [HPO term]
- Vascular dilatation [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- arteritis, familial granulomatous, with juvenile polyarthritis [MeSH Supplementary Concept]
- arteritis, familial granulomatous, with juvenile polyarthritis [MeSH concept]

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

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