hereditary spherocytosis type 4
hereditary spherocytosis that has material basis in an autosomal dominant mutation of SLC4A1 on chromosome 17q21.31
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hereditary spherocytosis type 4
Summary
hereditary spherocytosis type 4 is a rare disease[1].
Key Facts
- hereditary spherocytosis type 4's instance of is recorded as rare disease[2].
- hereditary spherocytosis type 4's instance of is recorded as class of disease[3].
- hereditary spherocytosis type 4's subclass of is recorded as hereditary spherocytosis[4].
- hereditary spherocytosis type 4's subclass of is recorded as genetic disease[5].
- hereditary spherocytosis type 4's subclass of is recorded as autosomal dominant disease[6].
- hereditary spherocytosis type 4's MeSH descriptor ID is recorded as C567208[7].
- hereditary spherocytosis type 4's OMIM ID is recorded as 612653[8].
- hereditary spherocytosis type 4's OMIM ID is recorded as 612653[9].
- hereditary spherocytosis type 4's Disease Ontology ID is recorded as DOID:0110919[10].
- hereditary spherocytosis type 4's genetic association is recorded as SLC4A1[11].
- hereditary spherocytosis type 4's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110919[12].
- hereditary spherocytosis type 4's exact match is recorded as http://identifiers.org/doid/DOID:0110919[13].
- hereditary spherocytosis type 4's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_822[14].
- hereditary spherocytosis type 4's UMLS CUI is recorded as C2675212[15].
- hereditary spherocytosis type 4's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- hereditary spherocytosis type 4's Mondo ID is recorded as MONDO_0012981[17].
- hereditary spherocytosis type 4's UniProt disease ID is recorded as DI-02324[18].