INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 13; MRT13

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Summary

Literature (0)

OMIM:613192 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 13; MRT13

Xenbase Genes: trappc9, trappc9.2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013173 - intellectual disability, autosomal recessive 13
MONDO:0019502 - autosomal recessive non-syndromic intellectual disability

MONDO:0013173 - intellectual disability, autosomal recessive 13

MONDO:0019502 - autosomal recessive non-syndromic intellectual disability

Disease Ontology (DO):

DOID:0050889 - non-syndromic intellectual disability

DOID:0050889 - non-syndromic intellectual disability