microcephalic osteodysplastic primordial dwarfism, type ii Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Microcephalic osteodysplastic primordial dwarfism type II (MOPDII) is a form of microcephalic primordial dwarfism (MPD; see this term) characterized by severe pre- and postnatal growth retardation, with marked microcephaly in proportion to body size, skeletal dysplasia, abnormal dentition, insulin resistance, and increased risk for cerebrovascular disease. (Orphanet Rare Disease Ontology, Orphanet_2637)
External Link http://www.omim.org/entry/210720
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Genes

1 genes associated with the microcephalic osteodysplastic primordial dwarfism, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
PCNT pericentrin