Disease #00437 (SWNTS2 (Schwannomatosis, type 2 (SWNTS2)), OMIM:615670)

Official abbreviation SWNTS2
Name Schwannomatosis, type 2 (SWNTS2)
OMIM ID 615670
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene LZTR1
Associated tissues -
Disease features -
Remarks -
Date created 2014-06-28 22:13:09 +02:00 (CEST)
Date last edited 2020-10-16 09:48:45 +02:00 (CEST)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00382166 182998 - - M ? Germany - - - - - SWNTS2 Schwannoma LZTR1 LZTR1 1 1 Andreas Laner
00414238 200506 - - M ? Germany - - - - - SWNTS2 Peripheral Schwannoma, Cafe-au-lait spot LZTR1 LZTR1 1 1 Andreas Laner
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