Scott syndrome
inherited blood coagulation disease
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Scott syndrome
Summary
Scott syndrome is a rare disease[1].
Key Facts
- Scott syndrome's instance of is recorded as rare disease[2].
- Scott syndrome's instance of is recorded as class of disease[3].
- Scott syndrome is a type of blood coagulation disease[4].
- Scott syndrome is a type of inherited blood coagulation disease[5].
- Scott syndrome is a type of rare hemorrhagic disorder due to a qualitative platelet defect[6].
- Scott syndrome's genetic association is recorded as ANO6[7].
- Scott syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111052[8].
- Scott syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111052[9].
- Scott syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_806[10].
- Scott syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].