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DO Term : Noonan syndrome with multiple lentigines 1 [DOID:0080548] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A Noonan syndrome with multiple lentigines that has_material_basis_in heterozygous mutation in the PTPN11 gene on chromosome 12q24.
  • synonyms:
  • LEOPARD syndrome 1,
  • 151100,
  • OMIM:151100
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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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