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Summary Literature (1)
DOID:0050569 - Seckel syndrome

Disease Ontology Definition:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability.

Synonyms: bird-headed dwarfism, Harper's syndrome, microcephalic primordial dwarfism, Virchow-Seckel dwarfism

Xenbase Genes : plk4, atrip, traip, cenpe, cep63, nin, cep152, atr, cpap, dna2, rbbp8, nsmce2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019342 - Seckel syndrome


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): autosomal recessive disease (is_a), syndrome (is_a)