INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BILLUART TYPE; MRXSBL

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Summary

Literature (0)

MIM:300486 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BILLUART TYPE; MRXSBL

Xenbase Genes: ophn1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010337 - mandibular process mesenchyme from head mesenchyme

MONDO:0010337 - mandibular process mesenchyme from head mesenchyme

Disease Ontology (DO):

DOID:0050888 - syndromic intellectual disability

DOID:0050888 - syndromic intellectual disability