CATCN21 (medical condition): A rare recessively inherited type of congenital cataract that is not associated with any other abnormality. Type 1 is caused by a mutation on chromosome 19q13.
See also:
Cataract, congenital nuclear, autosomal recessive 1:
»Introduction: Cataract, congenital nuclear, autosomal recessive 1
»Symptoms of Cataract, congenital nuclear, autosomal recessive 1
CATCN21: Another name for Cataract, congenital nuclear, autosomal recessive 1 (or close medical condition association).
»Introduction: Cataract, congenital nuclear, autosomal recessive 1
»Symptoms of Cataract, congenital nuclear, autosomal recessive 1
Some of the symptoms of CATCN21 incude:
Read more about symptoms of CATCN21 (Cataract, congenital nuclear, autosomal recessive 1)
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