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MIM:616739 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 51; MRT51
Xenbase Genes: hnmt
Human Disease Resource: OMIM
MONDO:0014759 - intellectual disability, autosomal recessive 51 |
MONDO:0019502 - autosomal recessive non-syndromic intellectual disability |
DOID:0081214 - autosomal recessive intellectual developmental disorder 51 |