Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C4025252
Disease: Abnormal nasal morphology
Abnormal nasal morphology 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C1328440
Disease: Abnormality of amino acid metabolism
Abnormality of amino acid metabolism 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C4023722
Disease: Abnormality of hair texture
Abnormality of hair texture 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C4023616
Disease: Abnormality of immune system physiology
Abnormality of immune system physiology 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C4025797
Disease: Abnormality of prenatal development or birth
Abnormality of prenatal development or birth 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C0262444
Disease: Abnormality of the dentition
Abnormality of the dentition 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C4021797
Disease: Abnormality of the thorax
Abnormality of the thorax 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C0241267
Disease: Absence of subcutaneous fat
Absence of subcutaneous fat 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C0600033
Disease: Acquired Kyphoscoliosis
Acquired Kyphoscoliosis 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C0234376
Disease: Action Tremor
Action Tremor 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.110 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C0002170
Disease: Alopecia
Alopecia 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C0238621
Disease: Aminoaciduria
Aminoaciduria 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C0002871
Disease: Anemia
Anemia 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C0339182
Disease: Ankyloblepharon
Ankyloblepharon 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C3279222
Disease: Aplasia/Hypoplasia of the cerebellum
Aplasia/Hypoplasia of the cerebellum 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C1859077
Disease: Aplasia/Hypoplasia of the nails
Aplasia/Hypoplasia of the nails 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C0003862
Disease: Arthralgia
Arthralgia 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C0004096
Disease: Asthma
Asthma 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C0004106
Disease: Astigmatism
Astigmatism 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C0004134
Disease: Ataxia
Ataxia 		0.100 Biomarker HPO

Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2
CUI: C0151514
Disease: Atrophic condition of skin
Atrophic condition of skin 		0.100 Biomarker HPO