Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0041834
Disease: Erythema
Erythema
0.100 Biomarker phenotype HPO
Ichthyosiform Erythroderma, Congenital
0.100 Biomarker disease HPO
CUI: C0086437
Disease: Joint laxity
Joint laxity
0.100 Biomarker phenotype HPO
CUI: C0152424
Disease: Common ventricle
Common ventricle
0.100 Biomarker disease HPO
CUI: C0240635
Disease: Byzanthine arch palate
Byzanthine arch palate
0.100 Biomarker disease HPO
CUI: C0266464
Disease: Polymicrogyria
Polymicrogyria
0.100 Biomarker disease HPO
CUI: C0266483
Disease: Pachygyria
Pachygyria
0.100 Biomarker disease HPO
CUI: C0345392
Disease: Congenital kyphoscoliosis
Congenital kyphoscoliosis
0.100 Biomarker disease HPO
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure
0.100 Biomarker phenotype HPO
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior
0.100 Biomarker phenotype HPO
CUI: C0431478
Disease: Posteriorly rotated ear
Posteriorly rotated ear
0.100 Biomarker disease HPO
Delayed speech and language development
0.100 Biomarker phenotype HPO
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
0.100 Biomarker disease HPO
CUI: C0575158
Disease: Kyphoscoliosis deformity of spine
Kyphoscoliosis deformity of spine
0.100 Biomarker disease HPO
CUI: C0595939
Disease: Stillbirth
Stillbirth
0.100 Biomarker phenotype HPO
CUI: C0600033
Disease: Acquired Kyphoscoliosis
Acquired Kyphoscoliosis
0.100 Biomarker disease HPO
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus
0.100 Biomarker disease HPO
CUI: C0700201
Disease: Dyssomnias
Dyssomnias
0.100 Biomarker disease HPO
CUI: C0851578
Disease: Sleep Disorders
Sleep Disorders
0.100 Biomarker group HPO
CUI: C0853087
Disease: Nail abnormality
Nail abnormality
0.100 Biomarker phenotype HPO
CUI: C0870082
Disease: Hyperkeratosis
Hyperkeratosis
0.100 Biomarker disease HPO
CUI: C0973461
Disease: Dysphasia
Dysphasia
0.100 Biomarker disease HPO
CUI: C1184923
Disease: Lumbar hyperlordosis
Lumbar hyperlordosis
0.100 Biomarker disease HPO
CUI: C1306503
Disease: Congenital exomphalos
Congenital exomphalos
0.100 Biomarker disease HPO
Congenital absence of kidneys syndrome
0.100 Biomarker disease HPO