H3-3A, H3.3 histone A, 3020

N. diseases: 134; N. variants: 4
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004106
Disease: Astigmatism
Astigmatism 		0.100 GeneticVariation disease CLINVAR
CUI: C0006157
Disease: Breech Presentation
Breech Presentation 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0009806
Disease: Constipation
Constipation 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		0.100 GeneticVariation disease CLINVAR
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders 		0.100 GeneticVariation group CLINVAR
CUI: C0015310
Disease: Exotropia
Exotropia 		0.100 GeneticVariation disease CLINVAR
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0023380
Disease: Lethargy
Lethargy 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0024636
Disease: Malocclusion
Malocclusion 		0.100 GeneticVariation disease CLINVAR
CUI: C0028738
Disease: Nystagmus
Nystagmus 		0.100 GeneticVariation disease CLINVAR
CUI: C0035229
Disease: Respiratory Insufficiency
Respiratory Insufficiency 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0036572
Disease: Seizures
Seizures 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0038379
Disease: Strabismus
Strabismus 		0.100 GeneticVariation disease CLINVAR
CUI: C0039231
Disease: Tachycardia
Tachycardia 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0042798
Disease: Low Vision
Low Vision 		0.100 GeneticVariation disease CLINVAR
CUI: C0221354
Disease: Frontal bossing
Frontal bossing 		0.100 GeneticVariation disease CLINVAR
CUI: C0221358
Disease: Long narrow head
Long narrow head 		0.100 GeneticVariation disease CLINVAR
CUI: C0221766
Disease: Diastasis recti
Diastasis recti 		0.100 GeneticVariation disease CLINVAR
CUI: C0234146
Disease: Absent reflex
Absent reflex 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0239234
Disease: Low set ears
Low set ears 		0.100 GeneticVariation disease CLINVAR
CUI: C0240379
Disease: Open mouth (finding)
Open mouth (finding) 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0264303
Disease: Laryngomalacia
Laryngomalacia 		0.100 GeneticVariation disease CLINVAR
CUI: C0265529
Disease: Plagiocephaly
Plagiocephaly 		0.100 GeneticVariation disease CLINVAR
CUI: C0265865
Disease: Mesocardia
Mesocardia 		0.100 GeneticVariation disease CLINVAR