ICD-10: H31.23
Gyrate atrophy, choroid
Related Diseases
monogenic disease
variable age at onset electroclinical syndrome
X-linked monogenic disease
autosomal dominant disease
autosomal recessive disease
Y-linked monogenic disease
autosomal genetic disease
guanidinoacetate methyltransferase deficiency
Kahrizi syndrome
janus kinase-3 deficiency
lambda 5 deficiency
homocarnosinosis
CEDNIK syndrome
chromosome 2p12-p11.2 deletion syndrome
MEDNIK syndrome
mitochondrial complex I deficiency
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