GenTIGSA Gene Database on Rare Genetic Disorders
  Beta Version
Warburg Micro Syndrome  
Disease Aliases (15)

Micro syndrome 1

Microcephaly, microcornea, congenital cataract, mental retardation, optic atrophy and hypogenitalism

Rab3gap1 warburg micro syndrome

Warbm

Warbm1

Warbm1 warburg micro syndrome 1

Warburg micro syndrome

Warburg micro syndrome 1; warbm1

Warburg sjo fledelius syndrome

Warburg micro syndrome 1

Warburg micro syndrome caused by mutation in rab3gap1

Warburg micro syndrome type 1

Warburg-sjo-fledelius syndrome

Microcephaly, microcornea, congenital cataract, intellectual disability, optic atrophy and hypogenitalism

Associated Genes (4)
 

NCBI-RefSeq:  TBC1D20   (TBC1 domain family member 20)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  RAB3GAP1   (RAB3 GTPase activating protein catalytic subunit 1)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  RAB3GAP2   (RAB3 GTPase activating non-catalytic protein subunit 2)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  RAB18   (RAB18, member RAS oncogene family)

External Links:  gnomAD browser   Ensembl   GeneCards

 


Cross-references of Warburg micro syndrome OMIM GARD Orphanet NCBI-GTR NCBI-MedGen MalaCards      MeSH Annotations