NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN IMAGING ABNORMALITIES; NEDMISBA

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Summary

Literature (0)

MIM:616486 - NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN IMAGING ABNORMALITIES; NEDMISBA

Xenbase Genes: mfsd2a

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014660 - microcephaly 15, primary, autosomal recessive
MONDO:0016660 - autosomal recessive primary microcephaly

MONDO:0014660 - microcephaly 15, primary, autosomal recessive

MONDO:0016660 - autosomal recessive primary microcephaly