Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0221355
Disease: Macrocephaly
Macrocephaly
0.100 Biomarker disease HPO
Small for gestational age (disorder)
0.100 Biomarker phenotype HPO
CUI: C0239174
Disease: Late tooth eruption
Late tooth eruption
0.100 Biomarker phenotype HPO
CUI: C0239937
Disease: Microscopic hematuria
Microscopic hematuria
0.100 Biomarker phenotype HPO
CUI: C0268731
Disease: Renal glomerular disease
Renal glomerular disease
0.100 Biomarker group HPO
CUI: C0302511
Disease: Small for gestational age fetus
Small for gestational age fetus
0.100 Biomarker phenotype HPO
CUI: C0423110
Disease: Downward slant of palpebral fissure
Downward slant of palpebral fissure
0.100 Biomarker phenotype HPO
CUI: C0426429
Disease: Broad nasal tip
Broad nasal tip
0.100 Biomarker phenotype HPO
CUI: C0426886
Disease: Tapering fingers (finding)
Tapering fingers (finding)
0.100 Biomarker phenotype HPO
CUI: C0427480
Disease: Elliptocytosis found
Elliptocytosis found
0.100 Biomarker phenotype HPO
Delayed speech and language development
0.100 Biomarker phenotype HPO
CUI: C0494475
Disease: Tonic - clonic seizures
Tonic - clonic seizures
0.100 Biomarker disease HPO
CUI: C0578038
Disease: Thin lips
Thin lips
0.100 Biomarker phenotype HPO
CUI: C0856975
Disease: Autistic behavior
Autistic behavior
0.100 Biomarker disease HPO
Attention deficit hyperactivity disorder
0.100 Biomarker disease HPO
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.100 Biomarker phenotype HPO
CUI: C1565489
Disease: Renal Insufficiency
Renal Insufficiency
0.100 Biomarker disease HPO
CUI: C1836542
Disease: Depressed nasal bridge
Depressed nasal bridge
0.100 Biomarker phenotype HPO
CUI: C1836543
Disease: Thick vermilion border
Thick vermilion border
0.100 Biomarker phenotype HPO
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion
0.100 Biomarker phenotype HPO
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril
0.100 Biomarker phenotype HPO
CUI: C1846151
Disease: Widened subarachnoid space
Widened subarachnoid space
0.100 Biomarker phenotype HPO
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance
0.100 Biomarker phenotype HPO
CUI: C1848207
Disease: Poor speech
Poor speech
0.100 Biomarker phenotype HPO
CUI: C1849340
Disease: Long palpebral fissure
Long palpebral fissure
0.100 Biomarker phenotype HPO