|OBO ID: DOID:0050569|
|Term Name:||Seckel syndrome||Search Ontology:|
|Definition:||A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. http://en.wikipedia.org/wiki/Seckel_syndrome|
|Ontology:||Human Disease (DOID:0050569)|
OTHER Seckel syndrome PAGES
GENES INVOLVED No data available
PHENOTYPE No data available
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