(Q916398)

Statements

instance of

rare disease

0 references

class of disease

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subclass of

lymphatic system disease

1 reference

stated in

Disease Ontology

retrieved

29 November 2020

Disease Ontology ID

DOID:4977

disease

0 references

image

Lymphedema.jpg
2,604 × 3,472; 1.3 MB

0 references

has effect

Stemmer sign

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health specialty

medical genetics

0 references

genetic association

VEGFC

1 reference

stated in

Mutation in vascular endothelial growth factor-C, a ligand for vascular endothelial growth factor receptor-3, is associated with autosomal dominant milroy-like primary lymphedema.

FLT4

1 reference

stated in

Hereditary lymphedema: evidence for linkage and genetic heterogeneity

GJC2

1 reference

stated in

GJC2 missense mutations cause human lymphedema

on focus list of Wikimedia project

WikiProject Medicine

0 references

WordLift URL

http://data.medicalrecords.com/medicalrecords/healthwise/lymphedema_pdq__supportive_care_-_patient_information_nci

1 reference

reference URL

https://www.medicalrecords.com/health-a-to-z/lymphedema-pdq-supportive-care-patient-information-nci-definition/

http://data.medicalrecords.com/medicalrecords/healthwise/lymphedema

1 reference

reference URL

https://www.medicalrecords.com/health-a-to-z/lymphedema-definition/

NCI Thesaurus ID

C3207

1 reference

stated in

Disease Ontology

retrieved

15 May 2019

Disease Ontology ID

DOID:4977

exact match

http://purl.obolibrary.org/obo/DOID_4977

1 reference

stated in

Disease Ontology

retrieved

29 November 2020

Disease Ontology ID

DOID:4977

http://identifiers.org/doid/DOID:4977

1 reference

stated in

Identifiers.org

reference URL

https://registry.identifiers.org/registry/doid

Commons category

Lymphedema

0 references

topic's main category

Category:Lymphedema

0 references

Identifiers