GenTIGSA Gene Database on Rare Genetic Disorders
  Beta Version

Lists of Rare Genetic Disorders      

Primary Intestinal Lymphangiectasia(Waldmann disease) 
An Unknown mode(s) within the Gastrointestinal disorders category
Reported Pathogenic variants
Candidate Gene Information
S.No. Name/GeneID Description Cytogentic Band Gene Location on genomic DNA Gene Length Exons Details Gene Cross-References
1 FOXC2/2303 forkhead box C2 16q24.1 Chr16, NC_000016.10
(86566829..86569728)
2900 nt 1 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

2 PROX1/5629 prospero homeobox 1 1q32.3 Chr1, NC_000001.11
(213983151..214041510)
58360 nt 9 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

Variant Information
Disorder Cross-References:                GTR          MalaCards          NORD     

Patient care services
Clinical Symptoms & Disabilities

Prevalence
Under development