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Chromosomal anomaly with epilepsy as a major feature

MedGen UID:: 831430
•Concept ID:: CN226719
•: Finding

Orphanet:

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MeSH
Orphanet

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVChromosomal anomaly with epilepsy as a major feature

Follow this link to review classifications for Chromosomal anomaly with epilepsy as a major feature in Orphanet.

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Chromosomal anomaly with epilepsy as a major feature
Chromosomal anomaly with epilepsy as a major feature

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