Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0598226
Disease: Harlequin type ichthyosis
Harlequin type ichthyosis
0.900 GermlineCausalMutation disease ORPHANET Premature terminal differentiation and a reduction in specific proteases associated with loss of ABCA12 in Harlequin ichthyosis. 19179616 2009
CUI: C0598226
Disease: Harlequin type ichthyosis
Harlequin type ichthyosis
0.900 GeneticVariation disease UNIPROT Compound heterozygous mutations including a de novo missense mutation in ABCA12 led to a case of harlequin ichthyosis with moderate clinical severity. 16675967 2006
CUI: C0598226
Disease: Harlequin type ichthyosis
Harlequin type ichthyosis
0.900 GeneticVariation disease UNIPROT ABCA12 is the major harlequin ichthyosis gene. 16902423 2006
CUI: C0598226
Disease: Harlequin type ichthyosis
Harlequin type ichthyosis
0.900 Biomarker disease GENOMICS_ENGLAND
CUI: C0598226
Disease: Harlequin type ichthyosis
Harlequin type ichthyosis
0.900 Biomarker disease GENOMICS_ENGLAND
CUI: C0598226
Disease: Harlequin type ichthyosis
Harlequin type ichthyosis
0.900 Biomarker disease CTD_human