All individuals with variants in gene CRIPT

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00004048 - PubMed: Shaheen 2014, Journal: Shaheen 2014 4-generation family, unaffected carrier parents, deceased sister M yes Saudi Arabia Arab - - - - DWFP characteristic facies, hypoplastic terminal phalanges, osteopenia, blind, profound global developmental delay, hypopigmented skin patches and talipes. Bifrontal subdural hygroma on brain MRI 1 4 Fowzan Alkuraya
00004051 - PubMed: Shaheen 2014, Journal: Shaheen 2014 4-generation family, unaffected carrier parents, deceased brother M yes Egypt Arab 00y00m70d - - - DWFP characteristic facies, hypoplastic terminal phalanges, osteopenia, albinoid fundus, markedly impaired retinal function, recurrent infections, PDA, persistent anemia (Hb 8.3 g/dl) with anisopoikilocytosis. MRI showed increase white matter signal and hypogenesis of corpus callosum 1 4 Fowzan Alkuraya
00396178 189380 - - F yes Syria - - - - - SSMCF Abnormal hair morphology, Cutis marmorata, Failure to thrive, Short stature, Microcephaly, Ulnar deviation of the hand or of fingers of the hand 1 1 Andreas Laner
00396202 patient PubMed: Leduc 2016 2-generation family, 1 affected, unaffected heterozygous carrier parents F - United States African-American - - - - ? see paper; ..., postnatal growth retardation, global developmental delay, frontal bossing, high forehead, sparse hair, sparse eyebrows; high myopia, admixed hyper- and hypopigmented macules face, arms, and legs, bilateral syndactyly 4–5 toes 2 1 Johan den Dunnen
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.