Genes associated with “NDAGSCW”

2 genes foundOpen Targets: neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter4 ClinVar P/LP variants
How are genes scored? (0–100 composite)
-5–15
ClinGen
0–15
HPO Freq
0–15
Open Targets
0–12
Phen2Gene
0–10
ClinVar
0–8
Constraint
0–8
Dosage
0–8
OMIM CS
0–8
PanelApp
0–5
OMIM
0–5
G2P
0–4
Breadth
Tiers:Strong Candidates (≥20)Consider (≥8)Possible (≥3)
Evidence dots:
HPOClinVarPhen2GeneOpen TargetsPanelApp
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Strong Candidates

1 gene
1
RAB11B →

RAB11B, member RAS oncogene family

25
score
GTR ↑

Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter

Frequency
-
P/LP Variants
4
OT Score
0.76

Consider

1 gene
13NDAGSCW

NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW

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Data aggregated from HPO/Monarch, ClinVar, OMIM (phenotypes + clinical synopsis), Open Targets, PanelApp, Phen2Gene, and Gene2Phenotype. Click a gene to view full details.