SIX3, SIX homeobox 3, 6496

N. diseases: 117; N. variants: 14
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1834877
Disease: HOLOPROSENCEPHALY 2 (disorder)
HOLOPROSENCEPHALY 2 (disorder) 		0.920 Biomarker disease CTD_human
CUI: C1834877
Disease: HOLOPROSENCEPHALY 2 (disorder)
HOLOPROSENCEPHALY 2 (disorder) 		0.920 Biomarker disease GENOMICS_ENGLAND
CUI: C1834877
Disease: HOLOPROSENCEPHALY 2 (disorder)
HOLOPROSENCEPHALY 2 (disorder) 		0.920 Biomarker disease GENOMICS_ENGLAND
CUI: C1834877
Disease: HOLOPROSENCEPHALY 2 (disorder)
HOLOPROSENCEPHALY 2 (disorder) 		0.920 CausalMutation disease CLINVAR
CUI: C0079541
Disease: Holoprosencephaly
Holoprosencephaly 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C0079541
Disease: Holoprosencephaly
Holoprosencephaly 		0.700 Biomarker disease HPO
CUI: C0266484
Disease: Schizencephaly
Schizencephaly 		0.610 Biomarker disease GENOMICS_ENGLAND
CUI: C0266484
Disease: Schizencephaly
Schizencephaly 		0.610 Biomarker disease GENOMICS_ENGLAND
CUI: C0266484
Disease: Schizencephaly
Schizencephaly 		0.610 Biomarker disease HPO
CUI: C0266484
Disease: Schizencephaly
Schizencephaly 		0.610 CausalMutation disease CLINVAR
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly 		0.500 GermlineCausalMutation disease ORPHANET
CUI: C0431363
Disease: Alobar Holoprosencephaly
Alobar Holoprosencephaly 		0.500 GermlineCausalMutation disease ORPHANET
CUI: C0751617
Disease: Semilobar Holoprosencephaly
Semilobar Holoprosencephaly 		0.500 GermlineCausalMutation disease ORPHANET
CUI: C2931870
Disease: Familial schizencephaly
Familial schizencephaly 		0.300 Biomarker disease CTD_human
CUI: C0242343
Disease: Panhypopituitarism
Panhypopituitarism 		0.110 Biomarker disease HPO
CUI: C0266667
Disease: Cyclocephaly
Cyclocephaly 		0.110 Biomarker disease HPO
CUI: C1840235
Disease: SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR
SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR 		0.110 Biomarker disease HPO
CUI: C0004096
Disease: Asthma
Asthma 		0.100 Biomarker disease HPO
CUI: C0008297
Disease: Choanal Atresia
Choanal Atresia 		0.100 Biomarker disease HPO
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		0.100 Biomarker disease HPO
CUI: C0009806
Disease: Constipation
Constipation 		0.100 Biomarker phenotype HPO
CUI: C0011848
Disease: Diabetes Insipidus
Diabetes Insipidus 		0.100 Biomarker disease HPO
CUI: C0013336
Disease: Dwarfism
Dwarfism 		0.100 Biomarker disease HPO
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation 		0.100 Biomarker phenotype HPO
CUI: C0018916
Disease: Hemangioma
Hemangioma 		0.100 Biomarker disease HPO