Stormorken syndrome
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Stormorken syndrome
Summary
Stormorken syndrome is a rare disease[1]. It is known by 9 alternative names across languages and contexts.[2]
Key Facts
- Stormorken syndrome's instance of is recorded as rare disease[3].
- Stormorken syndrome's instance of is recorded as class of disease[4].
- Helge Stormorken is named after Stormorken syndrome[5].
- Stormorken syndrome is a type of blood platelet disease[6].
- Stormorken syndrome is a type of syndromic constitutional thrombocytopenia[7].
- Stormorken syndrome is a type of genetic disease[8].
- Stormorken syndrome's ICD-9-CM is recorded as 759.89[9].
- Stormorken syndrome's genetic association is recorded as STIM1[10].
- Stormorken syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060354[11].
- Stormorken syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060354[12].
- Stormorken syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3204[13].
- Stormorken syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
Stormorken syndrome is known by 9 alternative names across languages and contexts.[2]