ICD-10: Q60.6

PSPH deficiency autosomal recessive disease Y-linked monogenic disease autosomal genetic disease iridogoniodysgenesis syndrome guanidinoacetate methyltransferase deficiency Kahrizi syndrome IMAGe syndrome janus kinase-3 deficiency organic acidemia Smith-McCort dysplasia renal-hepatic-pancreatic dysplasia omodysplasia ciliopathy acrorenal syndrome chromosomal deletion syndrome chromosome 10q23 deletion syndrome chromosome 16q22 deletion syndrome chromosome 18p deletion syndrome chromosome 19q13.11 deletion syndrome chromosome 2p12-p11.2 deletion syndrome chromosome 2q31.2 deletion syndrome chromosome 3q29 microdeletion syndrome chromosome 4q21 deletion syndrome stromal dystrophy obsolete anterior segment mesenchymal dysgenesis fetal encasement syndrome Christianson syndrome Potter's syndrome monogenic disease obsolete genetic disorder congenital adrenal insufficiency congenital disorder of glycosylation type I congenital disorder of glycosylation type II triple-A syndrome Boomerang dysplasia Athabaskan brainstem dysgenesis syndrome funisitis neonatal period electroclinical syndrome infancy electroclinical syndrome AGAT deficiency PHGDH deficiency PSAT deficiency