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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   biotin-responsive basal ganglia disease
  

Disease ID 1274
Disease biotin-responsive basal ganglia disease
Synonym
basal ganglia disease, biotin-responsive
bbgd
biotin-thiamine-responsive basal ganglia disease
biotin-thiamine-responsive basal ganglia disease (disorder)
encephalopathy, thiamine-responsive
thiamine metabolism dysfunction syndrome 2
thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive type)
thiamine transporter-2 deficiency
thiamine-responsive encephalopathy
thmd2
Orphanet
OMIM
DOID
UMLS
C1843807
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:1)
C0029089  |  ophthalmoplegia  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
80704  |  SLC19A3  |  CLINVAR;CTD_human;GHR;ORPHANET;UNIPROT
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:3)
2643  |  GCH1  |  2.617  |  DISEASES
113235  |  SLC46A1  |  3.679  |  DISEASES
1861  |  TOR1A  |  1.844  |  DISEASES
Locus
Symbol | Locus(Total Locus:1)
SLC19A3  |  2q36.3
Disease ID 1274
Disease biotin-responsive basal ganglia disease
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:2)
HP:0000544  |  CPEO  |  1
HP:0000602  |  Ophthalmoplegia  |  1
Disease ID 1274
Disease biotin-responsive basal ganglia disease
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:6)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs121917882NA80704SLC19A3umls:C1843807CLINVARNA0.481900093NASLC19A32227702251CT,A
rs121917884NA80704SLC19A3umls:C1843807CLINVARNA0.481900093NASLC19A32227688216TC
rs137852957NA80704SLC19A3umls:C1843807CLINVARNA0.481900093NASLC19A32227702189TC
rs137852958NA80704SLC19A3umls:C1843807CLINVARNA0.481900093NASLC19A32227698757CG
rs713993048NA80704SLC19A3umls:C1843807CLINVARNA0.481900093NASLC19A32227702299GT
rs786205213NA80704SLC19A3umls:C1843807CLINVARNA0.481900093NASLC19A32227702244-A
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.)
Disease ID 1274
Disease biotin-responsive basal ganglia disease
Case(Waiting for update.)