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DO Term : Bardet-Biedl syndrome 16 [DOID:0110138] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Bardet-Biedl syndrome that has_material_basis_in homozygous or compound heterozygous mutations in the SDCCAG8 gene on chromosome 1q43.

synonyms:
ICD10CM:Q87.89,
BBS16,
OMIM:615993,
615993

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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