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
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