achondrogenesis type IB
achondrogenesis that has material basis in mutation in the SLC26A2 gene which results in umbilical or inguinal hernia and a prominent rounded abdomen
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achondrogenesis type IB
Summary
achondrogenesis type IB is a class of disease[1]. It draws 2 Wikipedia views per month (class_of_disease category, ranking #631 of 1,968).[2]
Key Facts
- achondrogenesis type IB's instance of is recorded as class of disease[3].
- achondrogenesis type IB's subclass of is recorded as achondrogenesis[4].
- achondrogenesis type IB's subclass of is recorded as autosomal recessive disease[5].
- achondrogenesis type IB's OMIM ID is recorded as 600972[6].
- achondrogenesis type IB's KEGG ID is recorded as H02065[7].
- achondrogenesis type IB's Disease Ontology ID is recorded as DOID:0080055[8].
- achondrogenesis type IB's Orphanet ID is recorded as 93298[9].
- achondrogenesis type IB's health specialty is recorded as medical genetics[10].
- achondrogenesis type IB's genetic association is recorded as SLC26A2[11].
- achondrogenesis type IB's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080055[12].
- achondrogenesis type IB's exact match is recorded as http://identifiers.org/doid/DOID:0080055[13].
- achondrogenesis type IB's UMLS CUI is recorded as C0265274[14].
- achondrogenesis type IB's GARD rare disease ID is recorded as 460[15].
- achondrogenesis type IB's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- achondrogenesis type IB's Mondo ID is recorded as MONDO_0010966[17].
- achondrogenesis type IB's UniProt disease ID is recorded as DI-00019[18].
Why It Matters
achondrogenesis type IB draws 2 Wikipedia views per month (class_of_disease category, ranking #631 of 1,968).[2]