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Metadata
ID DOID:0070006
PURL http://purl.obolibrary.org/obo/DOID_0070006 Copy
Name Seckel syndrome 6
Definition A Seckel syndrome that has_material_basis_in homozygous mutation in the CEP63 gene on chromosome 3q22.
https://www.ncbi.nlm.nih.gov/pubmed/21983783
Xrefs

MIM:614728

Synonyms

SCKL6 [EXACT]

Parent Relationships

is_a Seckel syndrome

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