Proteinuria, chronic benign

Preferred Label : Proteinuria, chronic benign;

Symbol : PROCHOB;

CISMeF acronym : PROCHOB;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal recessive;

Molecular basis : Caused by mutation in the cubilin (intrinsic factor-cobalamin receptor) gene (602977.0007);

Laboratory abnormalities : Albuminuria, chronic; Proteinuria, chronic;

Prefixed ID : #618884;

Détails

Origin ID

618884;

UMLS CUI

C5394384;

Genes related to phenotype
- Cubilin [OMIM gene]
HPO term(s)
- Albuminuria [HPO term]
- Autosomal recessive inheritance [HPO term]
- Proteinuria [HPO term]
Not associated HPO term(s)
- Renal insufficiency [HPO term]
Semantic type(s)
- Finding [UMLS semantic type]

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

Vous pouvez consulter :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients