SALL4, spalt like transcription factor 4, 57167

N. diseases: 245; N. variants: 17
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1623209
Disease: Okihiro Syndrome
Okihiro Syndrome
1.000 Biomarker disease GENOMICS_ENGLAND
CUI: C1623209
Disease: Okihiro Syndrome
Okihiro Syndrome
1.000 Biomarker disease GENOMICS_ENGLAND
CUI: C1327918
Disease: Oculootoradial syndrome
Oculootoradial syndrome
0.610 Biomarker disease GENOMICS_ENGLAND
CUI: C1327918
Disease: Oculootoradial syndrome
Oculootoradial syndrome
0.610 Biomarker disease CTD_human
CUI: C1327918
Disease: Oculootoradial syndrome
Oculootoradial syndrome
0.610 Biomarker disease GENOMICS_ENGLAND
CUI: C0013261
Disease: Duane Retraction Syndrome
Duane Retraction Syndrome
0.500 Biomarker disease HPO
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
0.410 Biomarker group HPO
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.410 Biomarker phenotype GENOMICS_ENGLAND
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.410 Biomarker phenotype HPO
CUI: C0152427
Disease: Polydactyly
Polydactyly
0.300 Biomarker disease GENOMICS_ENGLAND
CUI: C4228778
Disease: Abnormality of radial ray
Abnormality of radial ray
0.300 Biomarker phenotype GENOMICS_ENGLAND
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
0.110 Biomarker group HPO
CUI: C0026010
Disease: Microphthalmos
Microphthalmos
0.110 Biomarker disease HPO
CUI: C0158761
Disease: Radioulnar Synostosis
Radioulnar Synostosis
0.110 Biomarker disease HPO
CUI: C1395852
Disease: Polydactyly preaxial type 1
Polydactyly preaxial type 1
0.110 Biomarker disease HPO
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate
0.100 Biomarker disease HPO
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
0.100 Biomarker phenotype HPO
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
0.100 Biomarker disease HPO
CUI: C0008297
Disease: Choanal Atresia
Choanal Atresia
0.100 Biomarker disease HPO
CUI: C0013336
Disease: Dwarfism
Dwarfism
0.100 Biomarker disease HPO
CUI: C0015469
Disease: Facial paralysis
Facial paralysis
0.100 Biomarker disease HPO
CUI: C0016202
Disease: Flatfoot
Flatfoot
0.100 Biomarker phenotype HPO
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss
0.100 Biomarker disease HPO
Sensorineural Hearing Loss (disorder)
0.100 Biomarker disease HPO
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease
0.100 Biomarker disease HPO