PedAM

Pediatric Disease Annotations & Medicines


	lipoprotein glomerulopathy

Disease ID	770
Disease	lipoprotein glomerulopathy
Synonym	lipoprotein glomerulopathy (disorder)
Orphanet	ORPHANET:329481
OMIM	OMIM:611771
UMLS	C2673196
SNOMED-CT	SNOMEDCT_US_2016_09_01:446923008
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:2) C0035078 \| renal failure \| 1 C0155765 \| microangiopathy \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:1) APOE \| 348 \| CLINVAR;CTD_human;ORPHANET;UNIPROT
Inferring Gene	Entrez_id \| Symbol \| Resource(Total Genes:1) 348 \| APOE \| infer
Text Mined Gene	(Waiting for update.)
Locus	Symbol \| Locus(Total Locus:1) APOE \| 19q13.32

Disease ID	770
Disease	lipoprotein glomerulopathy
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:1) HP:0000083 \| Renal insufficiency \| 1

Disease ID	770
Disease	lipoprotein glomerulopathy
Manually Symptom	UMLS \| Name(Total Manually Symptoms:1) C0087086 \| thrombi
Text Mined Symptom	(Waiting for update.)

Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)

All Snps(Total Genotypes:2)
snpId	pubmedId	geneId	geneSymbol	diseaseId	sourceId	sentence	score	Year	geneSymbol_dbSNP	CHROMOSOME	POS	REF	ALT
rs121918397	NA	348	APOE	umls:C2673196	CLINVAR	NA	0.493963088	NA	APOE	19	44908784	G	A,C
rs121918399	NA	348	APOE	umls:C2673196	CLINVAR	NA	0.493963088	NA	APOE	19	44907843	C	T

GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)

GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)

Mapped by lexical matching(Total Items:0)
(Waiting for update.)

Mapped by homologous gene(Total Items:0)
(Waiting for update.)

Chemical(Total Drugs:0)
(Waiting for update.)

FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)

FDA labeling changes(Total Drugs:0)
(Waiting for update.)

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