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Disease Ontology Browser
Seckel syndrome (DOID:0050569)
Alliance: disease page
Synonyms: bird-headed dwarfism; Harper's syndrome; microcephalic primordial dwarfism; Virchow-Seckel dwarfism
Alt IDs: OMIM:210600, OMIM:606744, OMIM:613676, OMIM:613823, OMIM:614728, OMIM:614851, OMIM:615807, ICD10CM:Q87.1, ORDO:808
Definition: An autosomal recessive disease characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability.

Disease References using Mouse Models (4)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.11
The Jackson Laboratory