Search Ontology:
Human Disease
factor X deficiency
- Term ID
- DOID:2222
- Synonyms
-
- disease, Stuart-Prower
- Definition
- A blood coagulation disease that is characterized by the partial or complete absence of factor X activity in the blood. https://rarediseases.org/rare-diseases/factor-x-deficiency/
- References
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- GARD:6404
- MESH:D005171
- MIM:227600
- NCI:C131632
- ORDO:328
- SNOMEDCT_US_2023_03_01:76642003
- UMLS_CUI:C0015519
- Ontology
- Human Disease ( DOID:2222 )
- is a type of
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Genes Involved
Zebrafish Models