DISEASES

Disease-gene associations mined from literature

Human genes for Seckel syndrome

Seckel syndrome [DOID:0050569]

A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability.

Synonyms:  Seckel syndrome,  DOID:0050569,  Seckel disease,  Seckel disorder,  Seckel syndromes ...

Linkouts:  OMIM #1 #2 #3 #4 #5 #6 #7 #8 #9