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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   epidermolysis bullosa simplex with muscular dystrophy
  

Disease ID 1576
Disease epidermolysis bullosa simplex with muscular dystrophy
Synonym
ebsmd
epidermolysa bullosa simplex and limb girdle muscular dystrophy
epidermolysis bullosa simplex and limb-girdle muscular dystrophy
md-ebs
mdebs
Orphanet
OMIM
UMLS
C2931072
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:2)
C0878544  |  cardiomyopathy  |  2
C0007193  |  dilated cardiomyopathy  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
5339  |  PLEC  |  CTD_human;ORPHANET
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:8)
197  |  AHSG  |  1.793  |  DISEASES
1308  |  COL17A1  |  2.066  |  DISEASES
1785  |  DNM2  |  1.927  |  DISEASES
26151  |  NAT9  |  4.125  |  DISEASES
5339  |  PLEC  |  7.2  |  DISEASES
81493  |  SYNC  |  2.515  |  DISEASES
23336  |  SYNM  |  2.352  |  DISEASES
7033  |  TFF3  |  2.343  |  DISEASES
Locus
Symbol | Locus(Total Locus:1)
PLEC  |  8q24.3
Disease ID 1576
Disease epidermolysis bullosa simplex with muscular dystrophy
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:3)
Disease ID 1576
Disease epidermolysis bullosa simplex with muscular dystrophy
Manually Symptom
UMLS  | Name(Total Manually Symptoms:1)
C0007193  |  dilated cardiomyopathy
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:1)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
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 1576
Disease epidermolysis bullosa simplex with muscular dystrophy
Case(Waiting for update.)