cataract 41
cataract that has material basis in heterozygous mutation in the WFS1 gene on chromosome 4p16
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cataract 41
Summary
cataract 41 is a developmental defect during embryogenesis[1].
Key Facts
- cataract 41's instance of is recorded as developmental defect during embryogenesis[2].
- cataract 41's instance of is recorded as rare disease[3].
- cataract 41's instance of is recorded as class of disease[4].
- cataract 41's subclass of is recorded as cataract[5].
- cataract 41's subclass of is recorded as autosomal dominant disease[6].
- cataract 41's OMIM ID is recorded as 116400[7].
- cataract 41's Disease Ontology ID is recorded as DOID:0110241[8].
- cataract 41's health specialty is recorded as medical genetics[9].
- cataract 41's genetic association is recorded as WFS1[10].
- cataract 41's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110241[11].
- cataract 41's exact match is recorded as http://identifiers.org/doid/DOID:0110241[12].
- cataract 41's UMLS CUI is recorded as C1861826[13].
- cataract 41's UMLS CUI is recorded as C3805412[14].
- cataract 41's ICD-10-CM is recorded as Q12.0[15].
- cataract 41's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- cataract 41's Mondo ID is recorded as MONDO_0007287[17].
- cataract 41's UniProt disease ID is recorded as DI-04010[18].