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HP and hemophilia are reported together in 1 article.
Gene
HP
- HGNC
- HGNC:5141
6articles
6mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
Hemophilia
122articles
122mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
1 records shown · first 60Detection of hemophilia by fluorescence spectroscopy: A photodiagnosis approach.
PMID 31731066 | DOI 10.1016/j.pdpdt.2019.101598 · Photodiagnosis and photodynamic therapy · 2020 · 2 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | HP | “Hemophilia (HP), the deficiency of clotting factors such as VIII (FVIII) and IX, is an inherited blood disorder which is due to the lack of clotting protein.” | 0.98 | hgnc_dict_v1 |
| phenotype | hemophilia | “Detection of hemophilia by fluorescence spectroscopy: A photodiagnosis approach.” | 0.98 | phenotype_alias_lexicon_v2 |