ICD-10: Z15.1
Genetic susceptibility to epilepsy and neurodevelopmental disorders
Coding Guidelines
Code Also
- developmental disorders of scholastic skills (F81.-)
- other neurodevelopmental disorder (F88)
- pervasive developmental disorders (F84.-)
- developmental disorder of speech and language (F80.-)
- developmental and epileptic encephalopathy (G93.45)
- intellectual disabilities (F70-F79)
- , if applicable, related disorders such as:
- epilepsy, by specific type (G40.-)
Related Diseases
chromosome 6q11-q14 deletion syndrome
chromosome 16p13.3 duplication syndrome
MEDNIK syndrome
Yunis-Varon syndrome
autosomal dominant nocturnal frontal lobe epilepsy 2
familial temporal lobe epilepsy 6
familial temporal lobe epilepsy 7
familial temporal lobe epilepsy 4
syndromic X-linked intellectual disability Hedera type
syndromic X-linked intellectual disability Abidi type
ABCD syndrome
infancy electroclinical syndrome
adenylosuccinase lyase deficiency
Ogden syndrome
recombinase activating gene 2 deficiency
Van Maldergem syndrome
pontocerebellar hypoplasia type 2A
mitochondrial complex V (ATP synthase) deficiency nuclear type 2
CEDNIK syndrome
Vici syndrome
chromosome 15q25 deletion syndrome
Medical Disclaimer: The information provided on this website is for general informational and educational purposes only.
It is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare provider with questions about your medical condition.