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Mental retardation, autosomal dominant 39
Mental retardation, autosomal dominant 39
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Subtype of:
Intellectual disability
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Show by gene
(one row per gene, with all of its disease terms together)
Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
Mental retardation, autosomal dominant 39
MONDO_0014678
MYT1L
Unknown
21990140
26240977
25126114
25232846
24129437
23033978
25529582
29293472
28859103
28470180
Open Targets
—
MRD39
MONDO_0014678
MYT1L
Unknown
23033978
26240977
25529582
29293472
25232846
28859103
28470180
Open Targets
—
All
1
Causal
0
Unknown
1
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
Open Targets
1
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Related via 1 shared gene including MYT1L.
1
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