Entry Search - 193300 608537 - OMIM
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Search: '193300 608537 (Search in: MIM number)'
Results: 2 entries.

1:
* 608537. VON HIPPEL-LINDAU TUMOR SUPPRESSOR; VHL
Cytogenetic location: 3p25.3, Genomic coordinates (GRCh38): 3:10,141,778-10,153,667
Matching terms: 608537
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
3p25.3 Erythrocytosis, familial, 2 263400 AR 3
Hemangioblastoma, cerebellar, somatic 3
Pheochromocytoma 171300 AD 3
Renal cell carcinoma, somatic 144700 3
von Hippel-Lindau syndrome 193300 AD 3
ICD+
SNOMEDCT: 46659004
ICD10CM: Q85.83

2:
# 193300. VON HIPPEL-LINDAU SYNDROME; VHLS
VON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED
Cytogenetic locations: 3p25.3, 11q13.3
Matching terms: 193300
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
3p25.3 von Hippel-Lindau syndrome 193300 AD 3 VHL 608537
11q13.3 {von Hippel-Lindau syndrome, modifier of} 193300 AD 3 CCND1 168461
ICD+
SNOMEDCT: 46659004
ICD10CM: Q85.83
ORPHA: 892
DO: 14175
Search: 193300 608537 (Search in: MIM number)
Results: 2 entries.

1:
* 608537. VON HIPPEL-LINDAU TUMOR SUPPRESSOR; VHL
Cytogenetic location: 3p25.3, Genomic coordinates (GRCh38): 3:10,141,778-10,153,667
Matching terms: 608537

2:
# 193300. VON HIPPEL-LINDAU SYNDROME; VHLS
VON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED
Cytogenetic locations: 3p25.3, 11q13.3
Matching terms: 193300