hereditary spherocytosis type 3
hereditary spherocytosis that has material basis in an autosomal dominant mutation of SPTA1 on chromosome 1q23.1
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hereditary spherocytosis type 3
Summary
hereditary spherocytosis type 3 is a class of disease[1].
Key Facts
- hereditary spherocytosis type 3's instance of is recorded as class of disease[2].
- hereditary spherocytosis type 3 is a type of hereditary spherocytosis[3].
- hereditary spherocytosis type 3 is a type of genetic disease[4].
- hereditary spherocytosis type 3 is a type of autosomal recessive disease[5].
- hereditary spherocytosis type 3's genetic association is recorded as SPTA1[6].
- hereditary spherocytosis type 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110918[7].
- hereditary spherocytosis type 3's exact match is recorded as http://identifiers.org/doid/DOID:0110918[8].
- hereditary spherocytosis type 3's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_822[9].
- hereditary spherocytosis type 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].