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DO Term : brittle cornea syndrome 2 [DOID:0080729] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An Ehlers-Danlos syndrome that has_material_basis_in homozygous mutation in the PRDM5 gene on chromosome 4q27.

synonyms:
614170,
OMIM:614170

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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