frontometaphyseal dysplasia 2

Any frontometaphyseal dysplasia in which the cause of the disease is a mutation in the MAP3K7 gene. [ MONDO:patterns/disease_series_by_gene ]

Preferred root terms

All terms

This is just here as a test because I lose it

database cross reference

abbreviation

FMD2 [ MONDOLEX:0014935 https://omim.org/entry/617137 ]

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/specific_disease_by_dysfunctional_structure.yaml

definition

Any frontometaphyseal dysplasia in which the cause of the disease is a mutation in the MAP3K7 gene.

exactMatch

http://linkedlifedata.com/resource/umls/id/C4310697

http://identifiers.org/omim/617137

http://purl.obolibrary.org/obo/DOID_0111787

has exact synonym

MAP3K7 frontometaphyseal dysplasia

frontometaphyseal dysplasia 2; FMD2

FMD2

Frontometaphyseal dysplasia type 2

frontometaphyseal dysplasia caused by mutation in MAP3K7

Frontometaphyseal dysplasia 2

MONDO:0014935

Equivalent to:

Subclass of: