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's subclass of is recorded as hereditary spherocytosis[3].
- hereditary spherocytosis type 3's subclass of is recorded as genetic disease[4].
- hereditary spherocytosis type 3's subclass of is recorded as autosomal recessive disease[5].
- hereditary spherocytosis type 3's MeSH descriptor ID is recorded as C567489[6].
- hereditary spherocytosis type 3's OMIM ID is recorded as 270970[7].
- hereditary spherocytosis type 3's Disease Ontology ID is recorded as DOID:0110918[8].
- hereditary spherocytosis type 3's genetic association is recorded as SPTA1[9].
- hereditary spherocytosis type 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110918[10].
- hereditary spherocytosis type 3's exact match is recorded as http://identifiers.org/doid/DOID:0110918[11].
- hereditary spherocytosis type 3's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_822[12].
- hereditary spherocytosis type 3's UMLS CUI is recorded as C2678338[13].
- hereditary spherocytosis type 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- hereditary spherocytosis type 3's Mondo ID is recorded as MONDO_0010053[15].
- hereditary spherocytosis type 3's UniProt disease ID is recorded as DI-02323[16].