Lymphatic Malformation 12 (LMPHM12)

Alias:
Central Conducting Lymphatic Anomaly
Lmphm12
Ccla
Lymphatic Malformation-7
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Lymphatic Malformation 12, also known as central conducting lymphatic anomaly, is related to capillary malformation-arteriovenous malformation 1 and lymphatic system disease. An important gene associated with Lymphatic Malformation 12 is MDFIC (MyoD Family Inhibitor Domain Containing), and among its related pathways/superpathways are Signal Transduction and Prolactin Signaling. Affiliated tissues include placenta and testis, and related phenotypes are lymphedema and fetal ascites
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
10
70
1

Medical Symptom

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

Gene & Mutation

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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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