Watson syndrome
Watson syndrome is an autosomal dominant condition characterized by Lisch nodules of the ocular iris, axillary/inguinal freckling, pulmonary valvular stenosis, relative macrocephaly, short stature, and neurofibromas.Watson syndrome is allelic to NF1, the same gene associated with neurofibromatosis type 1.
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Café au lait spotLaryngo-onycho-cutaneous syndromeLisch noduleList of OMIM disorder codesList of diseases (N)List of diseases (W)List of eponymous diseasesList of skin conditionsList of syndromesNeurofibromaNeurofibromatosis-Noonan syndromeNeurofibromatosis type INeurofibromin 1Noonan syndromeWesterhof syndrome
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Watson syndrome
Watson syndrome is an autosomal dominant condition characterized by Lisch nodules of the ocular iris, axillary/inguinal freckling, pulmonary valvular stenosis, relative macrocephaly, short stature, and neurofibromas.Watson syndrome is allelic to NF1, the same gene associated with neurofibromatosis type 1.
has abstract
Décrit en 1967, le syndrome de ...... nodules de Lisch est possible.
@fr
Watson syndrome is an autosoma ...... with neurofibromatosis type 1.
@en
متلازمة واطسون هي مرض صبغي الج ...... الليفي العصبي من النوع الأول.
@ar
沃森综合征（Watson syndrome）是一种常染色体显性遗传病。以虹膜色素缺陷瘤、腋窝/腹股沟斑点和神经纤维瘤形成为特点。 沃森综合征可能和引起的拥有相同的等位基因。
@zh
DiseasesDB
ICD10
MeSH ID
OMIM id
Wikipage page ID
24,167,376
page length (characters) of wiki page
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1,022,086,902
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DiseasesDB
ICD
@en
Q87.1
@en
MeshID
D009456
@en
name
Watson syndrome
@en
OMIM
Orphanet
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subject
hypernym
comment
Décrit en 1967, le syndrome de ...... nodules de Lisch est possible.
@fr
Watson syndrome is an autosoma ...... with neurofibromatosis type 1.
@en
متلازمة واطسون هي مرض صبغي الج ...... الليفي العصبي من النوع الأول.
@ar
沃森综合征（Watson syndrome）是一种常染色体显性遗传病。以虹膜色素缺陷瘤、腋窝/腹股沟斑点和神经纤维瘤形成为特点。 沃森综合征可能和引起的拥有相同的等位基因。
@zh
label
Syndrome de Watson
@fr
Watson syndrome
@en
متلازمة واطسون
@ar
沃森综合征
@zh
wasDerivedFrom
isPrimaryTopicOf
name
Watson syndrome
@en