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DO Term : Seckel syndrome 5 [DOID:0070012] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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

synonyms:
613823,
OMIM:613823,
SCKL5

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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