Disease-gene associations mined from literature

Human genes for Noonan syndrome with multiple lentigines

Noonan syndrome with multiple lentigines [DOID:14291]

A RASopathy that is characterized by autosomal dominant inheritance of brown skin spots called lentigines that are similar to freckles, heart defects, widely spaced eyes a sunken chest or protruding chest and short stature.

Synonyms:  Noonan syndrome with multiple lentigines,  DOID:14291,  Noonan syndrome with multiple lentigineses,  Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome,  Generalized lentiginosis ...

Linkouts:  OMIM #1 #2 #3 #4