Microcephalic Osteodysplastic Primordial Dwarfism, Type II Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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://ctdbase.org/detail.go?type=disease&acc=MESH:C565898
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1 genes/proteins associated with the disease Microcephalic Osteodysplastic Primordial Dwarfism, Type II from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
PCNT pericentrin 2.88009