ICD-10: Q89

acrofrontofacionasal dysostosis pontocerebellar hypoplasia type 2A pontocerebellar hypoplasia type 2C Ohdo syndrome, SBBYS variant oculodentodigital dysplasia acrofacial dysostosis Cincinnati type punctate palmoplantar keratoderma type III orofaciodigital syndrome VIII acrofacial dysostosis orofaciodigital syndrome IX acrofacial dysostosis Rodriguez type chondrodysplasia Blomstrand type chromosome 16q22 deletion syndrome anauxetic dysplasia 1 Baller-Gerold syndrome funisitis infancy electroclinical syndrome obsolete nonsyndromic epilepsy schneckenbecken dysplasia iridogoniodysgenesis syndrome proximal symphalangism tarsal-carpal coalition syndrome pancreatic agenesis IMAGe syndrome phalanx chondroma sacrum chordoma Mowat-Wilson syndrome Schimke immuno-osseous dysplasia lethal congenital contracture syndrome 2 Ritscher-Schinzel syndrome hypertrichotic osteochondrodysplasia Cantu type Nance-Horan syndrome obsolete anterior segment mesenchymal dysgenesis X-linked cleft palate with or without ankyloglossia ulnar-mammary syndrome fetal encasement syndrome congenital hereditary endothelial dystrophy of cornea restrictive dermopathy autosomal recessive Robinow syndrome congenital diarrhea hypomyelinating leukodystrophy Prieto syndrome syndromic X-linked intellectual disability Siderius type Hirata disease lacrimoauriculodentodigital syndrome 1 pachyonychia congenita Loeys-Dietz syndrome erythrokeratodermia variabilis obsolete acroosteolysis familial medullary thyroid carcinoma obsolete Majewski syndrome obsolete infantile onset spinocerebellar ataxia spondylocostal dysostosis congenital disorder of glycosylation type I Aland Island eye disease