hypomelination (Melissa Berry)

mgijax / mammalian-phenotype-ontology

Standard terms for annotating mammalian phenotypic data

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hypomelination (Melissa Berry) #503

Closed obophenotype-user closed 9 years ago

obophenotype-user commented 14 years ago

The term could be myelin deficiency or hypomyelination. Child of MP:0000920 (abnormal myelination), which has 241 genotypes, and sibling of demyelination. This particular mouse has a myelin deficiency in the CNS but normal myelination of PNS so you might want children of this term too.

Thank you,

Melissa

Reported by: cindyJax

Original Ticket: obo/mammalian-phenotype-requests/503

obophenotype-user commented 14 years ago

Paper J156938 could use it

Original comment by: jbubier

obophenotype-user commented 14 years ago

New term added:

MP:0010049 hypomyelination.

After surveying annotations, I'll see if more terms are warranted.

Original comment by: cindyJax

obophenotype-user commented 14 years ago

status: open --> pending

Original comment by: cindyJax

obophenotype-user commented 14 years ago

status: pending --> closed-accepted

Original comment by: cindyJax