cataract 42
Human disease
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cataract 42
Summary
cataract 42 is a developmental defect during embryogenesis[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- cataract 42's instance of is recorded as developmental defect during embryogenesis[3].
- cataract 42's instance of is recorded as rare disease[4].
- cataract 42's instance of is recorded as class of disease[5].
- cataract 42 is a type of cataract[6].
- cataract 42 is a type of autosomal dominant disease[7].
- cataract 42's health specialty is recorded as medical genetics[8].
- cataract 42's genetic association is recorded as CRYBA2[9].
- cataract 42's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110237[10].
- cataract 42's exact match is recorded as http://identifiers.org/doid/DOID:0110237[11].
- cataract 42's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
Why It Matters
cataract 42 is known by 5 alternative names across languages and contexts.[2]