ICD-10: H26.063

monogenic disease Alstrom syndrome Gamstorp-Wohlfart syndrome ABCD syndrome infancy electroclinical syndrome Ogden syndrome Kahrizi syndrome recombinase activating gene 1 deficiency lambda 5 deficiency Cogan-Reese syndrome Van Maldergem syndrome Ohdo syndrome, SBBYS variant CEDNIK syndrome ciliopathy Galloway-Mowat syndrome 1 chromosome 2q31.2 deletion syndrome chromosome 17q21.31 duplication syndrome stromal dystrophy MEDNIK syndrome Holzgreve-Wagner-Rehder Syndrome 3MC syndrome 1 3MC syndrome 2 3MC syndrome 3 Yunis-Varon syndrome obsolete anterior segment mesenchymal dysgenesis Muenke Syndrome