LD21.0
category
Syndromes with microphthalmia as a major feature
Definition
Syndromes in which abnormally small eyes form an important component.
Also indexed as
Anophthalmia - pulmonary hypoplasiaAnophthalmia or microphthalmia - oesophageal atresiaBakrania-Ragge syndromeMCOPS8MCOPS9 - [Syndromic microphthalmia type 9]MIDAS syndromeMMEP syndromeMatthew-Wood syndromeMicrocephaly - microphthalmia - ectrodactyly of lower limbs - prognathismMicrocephaly, microphthalmia, ectrodactyly of lower limbs, prognathism syndromeMicrophthalmia - ankyloblepharon - intellectual deficitMicrophthalmia - brain atrophyMicrophthalmia with limb anomaliesMicrophthalmia, Lenz typeMicrophthalmia, dermal aplasia, and sclerocorneaMicrophthalmia, dermal aplasia, and sclerocornea syndromeMicrophthalmos associated with Branchio-oculo-facial syndromeMicrophthalmos associated with Delleman syndromeMicrophthalmos associated with Fryns syndromeMicrophthalmos associated with GOMBOMicrophthalmos associated with Lenz microphthalmiaMicrophthalmos associated with MIDAS syndromeMicrophthalmos associated with growth retardation, ocular abnormalities, microcephaly, brachydactyly and oligophreniaMicrophthalmos associated with other syndromesMicrophthalmos associated with syndromesOculo-facio-cardio-dental syndromeOphthalmoacromelic syndromeSyndromes with microphthalmia as a major featureSyndromic microphthalmia due to OTX2 mutationSyndromic microphthalmia type 1Syndromic microphthalmia type 10Syndromic microphthalmia type 2Syndromic microphthalmia type 3Syndromic microphthalmia type 4Syndromic microphthalmia type 5Syndromic microphthalmia type 6Syndromic microphthalmia type 7Syndromic microphthalmia type 8Syndromic microphthalmia type 9Syndromic nanophthalmos with ADVIRC - [autosomal dominant vitreoretinochoroidopathy]Syndromic nanophthalmos with Kenny-Caffey syndromeSyndromic nanophthalmos with autosomal dominant vitreoretinochoroidopathyViljoen-Smart syndrome