FOXG1, forkhead box G1, 2290

N. diseases: 224; N. variants: 51
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		0.790 Biomarker disease CTD_human
CUI: C0025958
Disease: Microcephaly
Microcephaly 		0.500 Biomarker disease HPO
CUI: C0036572
Disease: Seizures
Seizures 		0.450 Biomarker phenotype HPO
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.410 Biomarker group HPO
CUI: C0013421
Disease: Dystonia
Dystonia 		0.400 Biomarker phenotype GENOMICS_ENGLAND
CUI: C0013421
Disease: Dystonia
Dystonia 		0.400 CausalMutation phenotype CLINVAR
CUI: C0013421
Disease: Dystonia
Dystonia 		0.400 Biomarker phenotype GENOMICS_ENGLAND
CUI: C0013421
Disease: Dystonia
Dystonia 		0.400 Biomarker phenotype HPO
CUI: C4305240
Disease: 14q12 microdeletion syndrome
14q12 microdeletion syndrome 		0.300 ChromosomalRearrangement disease ORPHANET
CUI: C4749855
Disease: 14q11.2 microduplication syndrome
14q11.2 microduplication syndrome 		0.300 ChromosomalRearrangement disease ORPHANET
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.150 Biomarker group HPO
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.150 CausalMutation disease CLINVAR
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability 		0.140 GeneticVariation disease CLINVAR
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability 		0.140 Biomarker disease HPO
CUI: C0175754
Disease: Agenesis of corpus callosum
Agenesis of corpus callosum 		0.120 Biomarker disease HPO
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		0.120 CausalMutation disease CLINVAR
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		0.120 Biomarker disease HPO
CUI: C0006325
Disease: Bruxism
Bruxism 		0.110 Biomarker phenotype HPO
CUI: C0008489
Disease: Chorea
Chorea 		0.110 Biomarker phenotype HPO
CUI: C0013384
Disease: Dyskinetic syndrome
Dyskinetic syndrome 		0.110 Biomarker disease HPO
CUI: C0003635
Disease: Apraxias
Apraxias 		0.100 Biomarker group HPO
CUI: C0004158
Disease: Athetosis
Athetosis 		0.100 Biomarker phenotype HPO
CUI: C0005744
Disease: Blepharophimosis
Blepharophimosis 		0.100 Biomarker disease HPO
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		0.100 Biomarker disease HPO
CUI: C0009806
Disease: Constipation
Constipation 		0.100 Biomarker phenotype HPO