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Genomic Search
Disease: OMIM
Disease: HPO
Examples Gene:
MT-ND1
,
POLG
, Region:
M:1-1000
Variant:
1:g.10042757T>C
,
rs3888511
, ClinVar:
RCV000000015
, Disease:
Leigh syndrome
, Phenotype:
Retinopathy
,
Human Phenotype Ontology
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SELECT DISTINCT t.id, t.name, t.acc FROM term2term AS t2t, term AS t WHERE t2t.term2_id='12103' AND t2t.term1_id=t.id ORDER BY t.name;