oculocerebral hypopigmentation syndrome, Cross type https://www.malacards.org/card/oculocerebral_syndrome_with_hypopigmentation Kramer syndrome OMIM:257800 ICD9:759.89 oculocerebral hypopigmentation syndrome MONDO:0009767 UMLS:C2936910 Oculocerebral hypopigmentation syndrome, Cross type is a rare congenital syndrome characterized by cutaneous and ocular hypopigmentation, various ocular anomalies (e.g. corneal and lens opacity, spastic ectropium, and/or nystagmus), growth deficiency, intellectual deficit and other progressive neurologic anomalies such as spastic tetraplegia, hyperreflexia, and/or athetoid movements. The clinical picture varies among patients and may also include other anomalies such as urinary tract abnormalities, Dandy-Walker malformations, and/or bilateral inguinal hernia. NORD:1520 GARD:0000105 SCTID:17827007 Oculocerebral Syndrome with Hypopigmentation hypopigmentation oculocerebral syndrome Cross type MEDGEN:423639 Cross syndrome Orphanet:2719 syndromic oculocutaneous albinism disorder of development or morphogenesis