Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/618884 http://purl.bioontology.org/ontology/OMIM/618884
Preferred Name	PROTEINURIA, CHRONIC BENIGN
Synonyms	PROCHOB
Type	http://www.w3.org/2002/07/owl#Class

altLabel	PROCHOB
prefLabel	PROTEINURIA, CHRONIC BENIGN
Gene Symbol	IFCR IGS1 CUBN
Scope Statement	Non-progressive disorder [MISCELLANEOUS] Benign condition [MISCELLANEOUS] Caused by mutation in the cubilin (intrinsic factor-cobalamin receptor) gene (602977.0007) [MOLECULAR BASIS] Onset in first decade [MISCELLANEOUS]
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU071183 http://purl.bioontology.org/ontology/OMIM/MTHU061868 http://purl.bioontology.org/ontology/OMIM/MTHU071182 http://purl.bioontology.org/ontology/OMIM/MTHU013583
tui	T033
Gene Locus	10p12.1
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	618884
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T033
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU000016
cui	C5394384
OMIM Entry Type	3
OMIM MimType Value	pound

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