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MORM syndrome
rareMORM syndrome is characterized by the association of intellectual deficit, truncal obesity, retinal dystrophy and micropenis. It has been described in 14 individuals from a consanguineous family. It is transmitted in an autosomal recessive manner. The causative locus has been mapped to chromosome region 9q34.
- Identifiers
- MONDO:0012423 OMIM:610156Orphanet:75858
- Causal genes
- INPP5E
- Part of
- Hereditary disease
- Also known as
- intellectual disability, truncal obesity, retinal dystrophy and micropenis · intellectual disability, truncal obesity, retinal dystrophy, and micropenis syndrome · intellectual disability-truncal obesity-retinal dystrophy-micropenis syndrome · mental retardation, truncal obesity, retinal dystrophy and micropenis · mental retardation, truncal obesity, retinal dystrophy, and micropenis
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