Terminology Service for NFDI4Health

obsolete_Cohen syndrome

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This term is obsolete


Reason for obsolescence

Replaced with Mondo term.

Replaced by

http://purl.obolibrary.org/obo/MONDO_0008999

Cohen syndrome (CS) is a rare genetic developmental disorder characterized by microcephaly, characteristic facial features, hypotonia, non-progressive intellectual deficit, myopia and retinal dystrophy, neutropenia and truncal obesity.

Term info

Label

obsolete_Cohen syndrome

database cross reference
reason for obsolescence

Replaced with Mondo term.

term replaced by

http://purl.obolibrary.org/obo/MONDO_0008999

Term relations

Subclass of: