Autosomal recessive mental retardation

Log in to bookmark this disease

Bookmark This Disease

Subtype of: Intellectual disability
Show the subtypes
Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Autosomal recessive mental retardation
MONDO_0019502
ARL14EP Unknown
21937992
Open Targets —
CACNA1G Unknown
21937992
Open Targets
EEF1B2 Unknown
24188901 21937992
Open Targets
ERLIN2 Unknown
21796390 23109142 22554690 23897027 27824013 23109145 25977983 23085305 21330303
Open Targets
FRY Unknown
31487712 21937992 27457812
Open Targets —
INPP4A Unknown
21937992
Open Targets
KDM6B Unknown
21937992
Open Targets
KIF7 Unknown
21937992
Open Targets
LAMA1 Unknown
25105227 21937992
Open Targets
LHX4-AS1 Unknown
21937992
Open Targets —
LINS1 Unknown
21937992 31922598 34450347 32499722 32802957 28181389 39138116 38563234 30090841 23773660
Open Targets —
MAN1B1 Unknown
24566669 26577042 21937992 24348268 26279649 21763484
Open Targets
NDST1 Unknown
21937992
Open Targets
POLR3B Unknown
21937992 33417887
Open Targets
PRRT2 Unknown
23126439 23352743 21937992 25595153 23398397 36180924 22543779 22744660 22243967
Open Targets —
SCAPER Unknown
21937992 28794130 28041643
Open Targets —
SLC31A1 Unknown
36562171 21937992 35913762
Open Targets
TTI2 Unknown
21937992 23956177
Open Targets —
UBR7 Unknown
33340455 21937992 36757286
Open Targets —
WDR45B Unknown
28503735 35322404 21937992
Open Targets
All20 Causal0 Unknown20
Related Diseases Diseases that share the most curated genes with Autosomal recessive mental retardation.
5 View disease cluster →
Al-gazali-bakalinova syndrome 1 shared geneKIF7 Related via 1 shared gene including KIF7. Spinocerebellar ataxia type 42 1 shared geneCACNA1G Related via 1 shared gene including CACNA1G. Developmental disorder with hypotonia, epilepsy, and cerebral/cerebellar atrophy 1 shared geneCACNA1G Related via 1 shared gene including CACNA1G. Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits 1 shared geneCACNA1G Related via 1 shared gene including CACNA1G. Cerebellar dysplasia with cysts with or without retinal dystrophy 1 shared geneLAMA1 Related via 1 shared gene including LAMA1.