ICD-10: Z15.8

autoimmune polyendocrine syndrome type 2 Charcot-Marie-Tooth disease type 1 Charcot-Marie-Tooth disease type 3 familial medullary thyroid carcinoma 2-hydroxyglutaric aciduria Dent disease Meckel syndrome orotic aciduria Townes-Brocks syndrome spinocerebellar ataxia type 10 recombinase activating gene 2 deficiency CD3gamma deficiency familial juvenile hyperuricemic nephropathy amyotrophic lateral sclerosis type 12 amyotrophic lateral sclerosis type 21 Baraitser-Winter syndrome Simpson-Golabi-Behmel syndrome type 1 congenital secretory chloride diarrhea 1 Rapp-Hodgkin syndrome hypoparathyroidism-retardation-dysmorphism syndrome hereditary papulotranslucent acrokeratoderma orofaciodigital syndrome III chromosome 14q11-q22 deletion syndrome chromosome 15q25 deletion syndrome chromosome 18p deletion syndrome chromosome 4q21 deletion syndrome chromosome 17q12 duplication syndrome Reis-Bucklers corneal dystrophy MEDNIK syndrome Pitt-Hopkins syndrome Kufor-Rakeb syndrome lethal congenital contracture syndrome 1 lethal congenital contracture syndrome 3 familial temporal lobe epilepsy 1 Griscelli syndrome type 1 Griscelli syndrome type 3