Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormal eye physiology (HP:0012373)

Parent Node:
Abnormality of vision (HP:0000504)

Parent Node:
Congenital stationary cone dysfunction (HP:0030637)

..Starting node
..Color vision defect (HP:0000551)

Term ID:	551
Name:	Color vision defect
Synonym:	Abnormal color vision; Abnormal colour vision; Abnormality of color vision; Abnormality of colour vision; Color vision defect, severe; Color vision defects; Colour vision defect; Colour vision defect, severe; Colour vision defects; Disturbed color vision; Loss in color vision; Loss in colour vision
Definition:	An anomaly in the ability to discriminate between or recognize colors.
Comments:
Reference:	HP:0000551
Genes and Diseases:	SELECT DISTINCT 'HP:0000551' AS Input, t2.acc as HPO_ID, t2.name as HPO_term, g.Distance, t1.Entrez_gene AS Gene, t1.Entrez_gene_id AS Gene_id_entrez, t1.HGNC_ID, t1.DiseaseId, t1.DiseaseName, t1.Frequency, t1.Onset #, t1.ConceptID, Source, t1.Typical_association , h.Variants AS HGMD_variants, c.variants AS ClinVar_variants FROM hpo202212.graph_path AS g, hpo202212.term AS t, hpo202212.term AS t2 LEFT JOIN hpo202212.hpo_phenotype_to_genes as t1 ON (t1.HPO = t2.acc) LEFT JOIN gb_exome.clinvar_variation_latest_sum AS c ON ( c.Gene = t1.Entrez_Gene) LEFT JOIN gb_exome.hgmd_allmumt_sum_latest AS h ON (h.gene = t1.Entrez_Gene ) WHERE (t.acc ='HP:0000551' AND g.term1_id = t.id AND g.distance <=20 AND t2.id = g.term2_id) order by g.distance, gene, DiseaseName;