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microcephaly 15, primary, autosomal recessive

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description A form of microcephaly, a disease defined as a head circumference more than 3 standard deviations below the age, sex and ethnically matched mean. Brain weight is markedly reduced and the cerebral cortex is disproportionately small.
Disease Ontology Description A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the MFSD2A gene on chromosome 1p34.
Mondo Term and Equivalent IDs
MONDO:0014660:  microcephaly 15, primary, autosomal recessive
UMLS:C4225310: