Online Mendelian Inheritance in Man

Last uploaded: January 31, 2024
Preferred Name

BROWN SYNDROME

Synonyms

BRWNS

ID

http://purl.bioontology.org/ontology/OMIM/616407

altLabel

BRWNS

cui

C0155339

Has manifestation

http://purl.bioontology.org/ontology/OMIM/MTHU051668

http://purl.bioontology.org/ontology/OMIM/MTHU051667

MIMTYPEMEANING

Mendelian phenotype or locus, molecular basis unknown.

notation

616407

OMIM Entry Type

5

OMIM MimType Value

perc

prefLabel

BROWN SYNDROME

Scope Statement

Noted in early childhood in most patients [MISCELLANEOUS]

Some patients have onset in second decade of life [MISCELLANEOUS]

tui

T047

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