Ltbp4-Related Cutis Laxa (URDS)

Alias:
Cutis Laxa with Severe Pulmonary, Gastrointestinal, and Urinary Abnormalities
Autosomal Recessive Cutis Laxa Type 1c
Urban-Rifkin-Davis Syndrome
Arcl1c
Urds
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Ltbp4-Related Cutis Laxa, also known as cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities, is related to cutis laxa, autosomal recessive, type ic and cutis laxa, and has symptoms including periorbital swelling Affiliated tissues include bone marrow and myeloid.
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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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
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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
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IF
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