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 4
Phenotype entries for this disease 4
Associated with 1 gene NF1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00377163 181704 - - M no Germany - - - - - 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
00448513 286660 - - M no Germany - - - - - NFNS Penile freckling, Long palpebral fissure, Micrognathia, Short stature, Motor delay, Thin upper lip vermilion, Broad nasal tip, Hypotonia NF1 NF1 1 1 Andreas Laner
00449778 - - - - - - - - - - - NFNS - NF1 NF1 1 1 Dan Feng Fang
00449779 - - - - - - - - - - - NFNS - NF1 NF1 1 1 Dan Feng Fang
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