Disease #00724 (NFNS (neurofibromatosis-Noonan syndrome (NFNS)), OMIM:601321)

Official abbreviation NFNS
Name neurofibromatosis-Noonan syndrome (NFNS)
OMIM ID 601321
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene NF1
Associated tissues -
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Individuals

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00377163 181704 - - M no Germany - - 0 - - NFNS Cafe-au-lait spot, Hypermelanotic macule, Multiple cafe-au-lait spots; Father and Grandmother also with multiple cafe-au-lait spots SPRED1 SPRED1 1 1 Andreas Laner
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