Disease

Microcephalic Osteodysplastic Primordial Dwarfism, Type II

About the Disease
Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii, also known as microcephalic osteodysplastic primordial dwarfism type ii, is related to isolated growth hormone deficiency and moyamoya disease 1. An important gene associated with Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii is PCNT (Pericentrin), and among its related pathways/superpathways are "Cell Cycle, Mitotic" and Loss of Nlp from mitotic centrosomes. Affiliated tissues include bone, brain and skin, and related phenotypes are delayed skeletal maturation and microcephaly

Common Targets
PCNT

疾病靶点研报
Microcephalic osteodysplastic primordial dwarfism, type II

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