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hereditary lymphedema I
Summary
- Synonym
-
- LMPH1
- Milroy disease
- Nonne-Milroy lymphedema
- PCL
- congenital primary lymphedema
- hereditary lymphedema type I
- Definition
- A hereditary lymphedema characterized by autosomal dominant inheritance of chronic, generally painless, lower limb lymphedema with onset typically at birth or in early childhood.
- Super Class
- hereditary lymphedema
External Links
- Disease Ontology
- DOID:0070212
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- ORDO
- GARD
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P13591 | Neural cell adhesion molecule 1 | |
| P15121 | Aldo-keto reductase family 1 member B1 | |
| P60484 | Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN |
