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GTR Home > Conditions/Phenotypes > Intellectual disability, autosomal recessive 66

Intellectual disability, autosomal recessive 66

Synonyms
Mental retardation, autosomal recessive 66

Summary

MRT66 is a nonsyndromic autosomal recessive intellectual developmental disorder with delayed speech development, neuropsychiatric symptoms, and relatively normal life span (Philips et al., 2017). [from OMIM]

Available tests

5 tests are in the database for this condition.

Clinical tests (5 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: C12orf4, Fy-3, MRT66, FERRY3
    Summary: FERRY endosomal RAB5 effector complex subunit 3

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

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