Disease #02770 (RPIAD (ribose-5-phosphate isomerase deficiency (RPIAD)), OMIM:608611)

Official abbreviation RPIAD
Name ribose-5-phosphate isomerase deficiency (RPIAD)
OMIM ID 608611
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene RPIA
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-08-25 17:21:16 +02:00 (CEST)


Individuals

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00226142 FamPatIII1 PubMed: Shukla 2019, Journal: Shukla 2019 3-generation family, unaffected heterozygous carrier parents M - India - - - - - RPIAD see paper; ..., developmental delay; speech delay; epilepsy; regression; dysarthria; no nystagmus; ataxia; spasticity; exaggerated deep tendon reflexes; extensor plantar reflex; increased urine polyol levels; retinitis pigmentosa; cerebral white matter abnormalities; no hearing loss; EEG slow right frontal discharge with epileptiform activity - ACIN1, ARHGAP28, CCDC59, DACH2, HAUS4, HOXA4, IDNK, MALRD1, MYH7B, NAA10, PCDHGA1, PCDHGA10, PCDHGA2, PCDHGA3, PCDHGA4, PCDHGA5, PCDHGA6, PCDHGA7, PCDHGA8, PCDHGA9, PCDHGB1, PCDHGB2, PCDHGB3, PCDHGB4, PCDHGB5, PCDHGB6, PPP1R12A, RPIA, TNNC2, UBE4B, ZNF628 17 1 Anju Shukla
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