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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
genetic disease +     
lymphedema +     
Aagenaes syndrome  
Adrenocortical Hypofunction, Chronic Primary Congenital 
adrenocorticotropic hormone deficiency  
advanced sleep phase syndrome 3  
age related macular degeneration 8  
Alpha-2-Deficient Collagen Disease 
Aquaporin 1 Deficiency  
ataxic cerebral palsy 
atrial heart septal defect 3  
atrial heart septal defect 4  
autoimmune lymphoproliferative syndrome +   
BOCKENHEIMER SYNDROME  
brachydactyly type A1B 
brachydactyly type A1C  
brachydactyly type A1D  
brachydactyly type B1  
brachydactyly type B2  
brachydactyly type E1  
brachydactyly type E2  
Breast Cancer Lymphedema +  
CADASIL +   
CAKUT2  
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
Cenani-Lenz syndactyly syndrome  
Choanal Atresia and Lymphedema  
chromosomal disease +   
complex cortical dysplasia with other brain malformations 1  
complex cortical dysplasia with other brain malformations 2  
complex cortical dysplasia with other brain malformations 3  
complex cortical dysplasia with other brain malformations 4  
complex cortical dysplasia with other brain malformations 5  
complex cortical dysplasia with other brain malformations 6  
Congenital Hepatic Fibrosis  
Congenital Pain Insensitivity +   
Dahlberg Borer Newcomer Syndrome 
desquamative interstitial pneumonia  
Dwarfism +   
ectodermal dysplasia and immunodeficiency 1  
elephantiasis +   
Familial Cirrhosis +   
Familial Dysalbuminemic Hyperthyroxinemia  
Familial Hemophagocytic Lymphohistiocytoses +   
familial hypertrophic cardiomyopathy +   
Familial Lipochrome Histiocytosis 
Familial Mixed Cryoglobulinemia  
Familial Temporal Epilepsy +   
frontotemporal dementia and/or amyotrophic lateral sclerosis 3  
frontotemporal dementia and/or amyotrophic lateral sclerosis 4  
Genetic Skin Diseases +   
German Syndrome 
Hennekam syndrome +   
Hereditary Bilateral Parotidomegaly 
Hereditary Epistaxis 
Hereditary Eye Diseases +   
hereditary lymphedema +   
A lymphedema commonly located_in legs, caused_by congenital abnormalities in the lymphatic system. (DO)
Hereditary Neoplastic Syndromes +   
hypotrichosis-lymphedema-telangiectasia syndrome +   
inherited metabolic disorder +   
Isolated Prolactin Deficiency 
Kallmann syndrome +   
Laminopathies +   
Lymphedema and Cerebral Arteriovenous Anomaly 
Lymphedema, Cardiac Septal Defects, and Characteristic Facies 
lymphedema-distichiasis syndrome +   
Marfan syndrome +   
microcephaly with or without chorioretinopathy, lymphedema, or mental retardation  
monogenic disease +   
Nervous System Heredodegenerative Disorders +   
Non-Filarial Lymphedema 
Nonimmune Chronic Idiopathic Neutropenia, Adult  
polygenic disease +   
primary hypertrophic osteoarthropathy +   
Primary Lymphedema with Myelodysplasia  
progressive familial intrahepatic cholestasis +   
Sacral Agenesis with Vertebral Anomalies  
Waldmann Disease 
yellow nail syndrome +  

Synonyms
Exact Synonyms: PCL ;   congenital familial lymphedema ;   congenital hereditary lymphedema ;   congenital hereditary lymphedemas ;   hereditary lymphedemas ;   primary congenital lymphedema ;   primary congenital lymphedemas
Narrow Synonyms: congenital recessive lymphedema
Alternate IDs: MESH:C565432
Xrefs: GARD:7220 ;   ICD9CM:757.0 ;   MIM:PS153100
Definition Sources: http://en.wikipedia.org/wiki/Milroy%27s_disease "DO" "DO"

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