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DO Term : MLS syndrome [DOID:0111875] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A syndrome characterized by linear skin defects and various other congenital anomalies. The classical diagnosis consisted of unilateral or bilateral microphthalmia and/or anophthalmia and linear skin defects but patients with a molecular diagnosis of MLS syndrome may not display eye abnormalities.
  • synonyms:
  • linear skin defects with multiple congenital anomalies,
  • PS309801,
  • OMIM:PS309801
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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