DISEASES

Disease-gene associations mined from literature

Human genes for Seckel syndrome 5

Seckel syndrome 5 [DOID:0070012]

A Seckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CEP152 gene on chromosome 15q21.

Synonyms:  Seckel syndrome 5,  DOID:0070012,  SCKL5