CAKUT2
CAKUT that has material basis in heterozygous mutation in the TBX18 gene on chromosome 6q14
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CAKUT2
Summary
CAKUT2 is a rare disease[1].
Key Facts
- CAKUT2's instance of is recorded as rare disease[2].
- CAKUT2's instance of is recorded as class of disease[3].
- CAKUT2's subclass of is recorded as CAKUT[4].
- CAKUT2's OMIM ID is recorded as 143400[5].
- CAKUT2's Disease Ontology ID is recorded as DOID:0080207[6].
- CAKUT2's Orphanet ID is recorded as 2190[7].
- CAKUT2's NCI Thesaurus ID is recorded as C99007[8].
- CAKUT2's genetic association is recorded as TBX18[9].
- CAKUT2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080207[10].
- CAKUT2's exact match is recorded as http://identifiers.org/doid/DOID:0080207[11].
- CAKUT2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2190[12].
- CAKUT2's UMLS CUI is recorded as C1840451[13].
- CAKUT2's GARD rare disease ID is recorded as 9517[14].
- CAKUT2's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- CAKUT2's Mondo ID is recorded as MONDO_0027676[16].
- CAKUT2's UniProt disease ID is recorded as DI-04535[17].