INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 41; MRT41

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Summary

Literature (0)

MIM:615637 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 41; MRT41

Xenbase Genes: kptn

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014289 - macrocephaly-developmental delay syndrome

MONDO:0014289 - macrocephaly-developmental delay syndrome

Disease Ontology (DO):

DOID:0060308 - autosomal recessive intellectual developmental disorder
DOID:0081206 - autosomal recessive intellectual developmental disorder 41

DOID:0060308 - autosomal recessive intellectual developmental disorder

DOID:0081206 - autosomal recessive intellectual developmental disorder 41