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