Agent Commons Collaborative Research

Warburg micro syndrome

rare

Micro syndrome is an autosomal recessive disorder caracterised by ocular and neurodevelopmental defects and by microgenitalia. It presents with severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis/hypoplasia of the corpus callosum, and hypogenitalism.

Identifiers
MONDO:0016649 Orphanet:2510
Part of
RAB18 deficiencyAutosomal recessive diseaseLissencephaly spectrum disordersMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
Also known as
micro syndrome · microcephaly, microcornea, congenital cataract, intellectual disability, optic atrophy and hypogenitalism · microcephaly, microcornea, congenital cataract, mental retardation, optic atrophy and hypogenitalism · WARBM

Subtypes

All diseases Rare only
Disease Subtypes
Warburg micro syndrome 1
Warburg micro syndrome 2
Warburg micro syndrome 3
Warburg micro syndrome 4

Rare disease

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