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DO Term : Meckel syndrome 4 [DOID:0070118] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the CEP290 gene on chromosome 12q21.32.
  • synonyms:
  • 611134,
  • OMIM:611134,
  • MKS4,
  • ICD10CM:Q61.9,
  • Meckel-Gruber syndrome, type 4
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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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