hereditary spherocytosis type 5
hereditary spherocytosis that has material basis in a mutation of EPB42 on chromosome 15q15.2
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hereditary spherocytosis type 5
Summary
hereditary spherocytosis type 5 is a rare disease[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- hereditary spherocytosis type 5's instance of is recorded as rare disease[3].
- hereditary spherocytosis type 5's instance of is recorded as class of disease[4].
- hereditary spherocytosis type 5 is a type of hereditary spherocytosis[5].
- hereditary spherocytosis type 5 is a type of genetic disease[6].
- hereditary spherocytosis type 5 is a type of autosomal recessive disease[7].
- hereditary spherocytosis type 5's genetic association is recorded as EPB42[8].
- hereditary spherocytosis type 5's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110920[9].
- hereditary spherocytosis type 5's exact match is recorded as http://identifiers.org/doid/DOID:0110920[10].
- hereditary spherocytosis type 5's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_822[11].
- hereditary spherocytosis type 5's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
Why It Matters
hereditary spherocytosis type 5 is known by 7 alternative names across languages and contexts.[2]