cataract 30
cataract that has material basis in heterozygous mutation in the VIM gene on chromosome 10p13
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cataract 30
Summary
cataract 30 is a developmental defect during embryogenesis[1].
Key Facts
- cataract 30's instance of is recorded as developmental defect during embryogenesis[2].
- cataract 30's instance of is recorded as rare disease[3].
- cataract 30's instance of is recorded as class of disease[4].
- cataract 30's subclass of is recorded as cataract[5].
- cataract 30's subclass of is recorded as autosomal dominant disease[6].
- cataract 30's OMIM ID is recorded as 116300[7].
- cataract 30's Disease Ontology ID is recorded as DOID:0110248[8].
- cataract 30's Orphanet ID is recorded as 98984[9].
- cataract 30's health specialty is recorded as medical genetics[10].
- cataract 30's genetic association is recorded as VIM[11].
- cataract 30's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110248[12].
- cataract 30's exact match is recorded as http://identifiers.org/doid/DOID:0110248[13].
- cataract 30's UMLS CUI is recorded as C1861827[14].
- cataract 30's UMLS CUI is recorded as C3805411[15].
- cataract 30's UMLS CUI is recorded as C1833118[16].
- cataract 30's ICD-10-CM is recorded as Q12.0[17].
- cataract 30's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
- cataract 30's Mondo ID is recorded as MONDO_0007286[19].
- cataract 30's UniProt disease ID is recorded as DI-03825[20].