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DOID:0050569 - Seckel syndrome
Disease Ontology Definition:An autosomal recessive disease characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability.
Synonyms: Harper's syndrome, Virchow-Seckel dwarfism, bird-headed dwarfism, microcephalic primordial dwarfism,
Echinobase Genes
:
cep63,
cep152,
dna2
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal recessive disease (is_a)