Watson Syndrome (WTSN)

Alias:
Wtsn
Café-Au-Lait Macules with Pulmonary Stenosis
Cafe-Au-Lait Macules with Pulmonary Stenosis
Pulmonary Stenosis with Cafe-Au-Lait Spots
Pulmonic Stenosis with Cafe-Au-Lait Spots
Cafe-Au-Lait Spots with Pulmonic Stenosis
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Watson Syndrome, also known as wtsn, is related to alagille syndrome 1 and alagille syndrome 2. An important gene associated with Watson Syndrome is NF1 (Neurofibromin 1). Affiliated tissues include breast, and related phenotypes are low-set ears and multiple cafe-au-lait spots
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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1
21
22

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
No Data Found!
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