|
gptkb:Hereditary_hemorrhagic_telangiectasia
|
Orphanet:774
|
|
gptkb:von_Hippel-Lindau_disease
|
gptkb:MedlinePlus:_Von_Hippel-Lindau_disease
|
|
gptkb:von_Hippel-Lindau_disease
|
gptkb:DOID:0050425
|
|
gptkb:von_Hippel-Lindau_disease
|
gptkb:SNOMED_CT:_109981000119104
|
|
gptkb:transfer_RNA_(tRNA)
|
Rfam
|
|
gptkb:Cowden_syndrome
|
gptkb:Orphanet
|
|
gptkb:von_Hippel-Lindau_disease
|
gptkb:Mondo:0008315
|
|
gptkb:transfer_RNA_(tRNA)
|
gptkb:Ensembl
|
|
gptkb:von_Hippel-Lindau_disease
|
gptkb:Genetics_Home_Reference:_Von_Hippel-Lindau_disease
|
|
gptkb:Hereditary_hemorrhagic_telangiectasia
|
MedlinePlus:001223
|
|
gptkb:transfer_RNA_(tRNA)
|
gptkb:NCBI_Gene
|
|
gptkb:VHL_syndrome
|
Genetics Home Reference: VHL
|
|
gptkb:von_Hippel-Lindau_disease
|
GARD: Von Hippel-Lindau disease
|
|
gptkb:von_Hippel-Lindau_disease
|
gptkb:HPO:0002616
|
|
gptkb:Hereditary_hemorrhagic_telangiectasia
|
GARD:0008702
|
|
gptkb:von_Hippel-Lindau_disease
|
gptkb:UMLS:C0042790
|
|
gptkb:VHL_syndrome
|
MedlinePlus: VHL syndrome
|
|
gptkb:von_Hippel-Lindau_disease
|
gptkb:Orphanet:_Von_Hippel-Lindau_disease
|
|
gptkb:Cowden_syndrome
|
gptkb:Genetics_Home_Reference
|
|
gptkb:von_Hippel-Lindau_disease
|
gptkb:MeSH:D014839
|