STS, steroid sulfatase, 412

N. diseases: 382; N. variants: 16
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0079588
Disease: Ichthyosis, X-Linked
Ichthyosis, X-Linked
0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C0079588
Disease: Ichthyosis, X-Linked
Ichthyosis, X-Linked
0.800 CausalMutation disease CLINVAR
Attention deficit hyperactivity disorder
0.460 Biomarker disease HPO
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
0.310 Biomarker disease HPO
CUI: C0020757
Disease: Ichthyoses
Ichthyoses
0.200 Biomarker disease HPO
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.200 Biomarker group HPO
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
0.190 Biomarker group HPO
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.130 Biomarker disease HPO
CUI: C0020619
Disease: Hypogonadism
Hypogonadism
0.120 Biomarker disease HPO
Ichthyosiform Erythroderma, Congenital
0.120 Biomarker disease HPO
CUI: C0013336
Disease: Dwarfism
Dwarfism
0.110 Biomarker disease HPO
CUI: C0036572
Disease: Seizures
Seizures
0.110 Biomarker phenotype HPO
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity
0.100 Biomarker phenotype HPO
CUI: C0020620
Disease: Hypohidrosis
Hypohidrosis
0.100 Biomarker disease HPO
CUI: C0036631
Disease: Seminoma
Seminoma
0.100 Biomarker disease HPO
CUI: C0037822
Disease: Speech Disorders
Speech Disorders
0.100 Biomarker group HPO
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.100 Biomarker disease HPO
CUI: C0151908
Disease: Dry skin
Dry skin
0.100 Biomarker phenotype HPO
CUI: C0238577
Disease: Abdominal wall defect
Abdominal wall defect
0.100 Biomarker group HPO
CUI: C0266294
Disease: Unilateral agenesis of kidney
Unilateral agenesis of kidney
0.100 Biomarker disease HPO
CUI: C0266463
Disease: Lissencephaly
Lissencephaly
0.100 Biomarker disease HPO
CUI: C0349588
Disease: Short stature
Short stature
0.100 Biomarker phenotype HPO
CUI: C0423250
Disease: Corneal stromal opacities
Corneal stromal opacities
0.100 Biomarker phenotype HPO
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
0.100 Biomarker disease HPO
CUI: C0870082
Disease: Hyperkeratosis
Hyperkeratosis
0.100 Biomarker disease HPO