Lymphangioma

Symptom Information:

Symptom ID: HPO:0100764
Synonyms:
Lymphangioma, no ICD-O subtype (morphologic abnormality) [Orphanet:36600]
Lymphangioma (disorder) [Orphanet:36600]
Congenital lymphangioma (disorder) [Orphanet:36600]
Benign lymphangioma (morphologic abnormality) [Orphanet:36600]
Lymphangioma [Orphanet:36600]
Lymphangioma [OMIM:Lymphangioma]
Lymphangioma/lymphatic malformations [Orphanet:36600]
Lymphangioma [MedDRA:10025219]
Lymphangioma, any site [MedDRA:10025219]
Lymphangiomatosis [MedDRA:10025219]
Quality:
Cross references:
Orphanet:36600 "Lymphangioma/lymphatic malformations" [Orphanet:36600]
OMIM: "Lymphangioma" [OMIM:Lymphangioma]
UMLS:C0024221 "Lymphangioma" [Orphanet:36600]
Is a (Direct Parents):
HPO         Abnormality of the lymphatic system
MedDRA Soft tissue neoplasms benign NEC
Orphanet Abnormality of the lymphatic system
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of the lymphatic system(HPO:0100763)
             Lymphangioma(HPO:0100764)
MedDRA:
Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104)
    Soft tissue neoplasms benign(MedDRA:10041294)
       Soft tissue neoplasms benign NEC(MedDRA:10041295)
          Lymphangioma(HPO:0100764)
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Angio-osteohypertrophic syndrome (Orphanet:2346)
CLAPO syndrome (Orphanet:168984)
Cobb syndrome (Orphanet:53721)
Enchondromatosis (Orphanet:296)
Hennekam syndrome (Orphanet:2136)
Hypotrichosis - lymphedema - telangiectasia (Orphanet:69735)
Klippel-Trénaunay syndrome (Orphanet:90308)
Knobloch syndrome (Orphanet:1571)
Proteus syndrome (Orphanet:744)
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus (Orphanet:137608)
Tuberous sclerosis (Orphanet:805)