GenTIGSA Gene Database on Rare Genetic Disorders

Lists of Rare Genetic Disorders  

Developmental And Epileptic Encephalopathy, 35(ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement)      Explore Disorder's Alias
An Autosomal recessive mode(s) within the Neurodevelopmental 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 ITPA/3704 inosine triphosphatase 20p13 Chr20, NC_000020.11
(3204065..3227449)
23385 nt 13 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

Variant Information       
Disorder Cross-References:      Orphanet          OMIM          GARD          GTR          MedGen          MalaCards          EMBL-EBI OLS    Monarch Initiative          NORD     

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Clinical Symptoms & Disabilities