multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome obsolete non-syndromic developmental defect of the eye syndromic microphthalmia microphthalmia, Lenz type NORD:1359 microphthalmia Lenz type A very rare X-linked inherited form of syndromic microphthalmia characterized by unilateral or bilateral microphthalmia (and/or clinical anophthalmia) with or without coloboma in addition to a range of extraocular manifestations such as microcephaly, malformed ears, dental abnormalities (i.e. irregular shape of incisors), skeletal anomalies (duplicated thumbs, syndactyly, clinodactyly, camptodactyly), urogenital anomalies (hypospadias, cryptorchidism, renal dysgenesis, hydroureter) and mild to severe intellectual disability. It is allelic to two disorders: oculofaciocardiodental syndrome and premature aging appearance-developmental delay-cardiac arrhythmia syndrome. MAA (formerly) GARD:0000087 MCOPS1 microphthalmia syndromic 1 icd11.foundation:678242327 MONDO:0018924 Lenz microphthamia syndrome syndromic microphthalmia type 1 microphthalmia or anophthalmos with associated anomalies (formerly) Orphanet:568 Editors note: TODO check Lenz microphthalmia Lenz dysplasia X-linked syndromic intellectual disability obsolete lens shape anomaly NAA10-related syndrome