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Summary Literature (0)
MIM:300990 - MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN

Xenbase Genes: ammecr1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010516 - midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis

Disease Ontology (DO):
DOID:0111859 - midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis