Cystic hygroma

Symptom Information:

Symptom ID: HPO:0000476
Synonyms:
Cystic hygroma of the neck [HPO:0000476]
Cystic lymphangioma (morphologic abnormality) [Orphanet:14600]
Cystic hygroma (disorder) [Orphanet:14600]
Non-neoplastic hygroma (disorder) [Orphanet:14600]
Lymphangioma, Cystic [Orphanet:14600]
Cystic hygroma [OMIM:Cystic hygroma]
Cystic hygroma [Orphanet:14600]
Cystic lymphangioma [Orphanet:14600]
Cystic lymphangioma [MedDRA:10058949]
Cystic hygroma [MedDRA:10058949]
Hygroma cystic [MedDRA:10058949]
Quality:
Cross references:
HPO:0010878 "Fetal cystic hygroma" [Orphanet:14600]
Orphanet:14600 "Cystic hygroma" [Orphanet:14600]
OMIM: "Cystic hygroma" [OMIM:Cystic hygroma]
UMLS:C0206620 "Lymphangioma, Cystic" [Orphanet:14600]
Is a (Direct Parents):
Orphanet Abnormality of the neck
HPO         Abnormality of the neck
MedDRA Soft tissue neoplasms benign NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the neck(HPO:0000464)
             Cystic hygroma(HPO:0000476)
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)
          Cystic hygroma(HPO:0000476)
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

Achondrogenesis (Orphanet:932)
Achondrogenesis type 1A (Orphanet:93299)
Achondrogenesis type 1B (Orphanet:93298)
Achondrogenesis type 2 (Orphanet:93296)
CATEL-MANZKE SYNDROME (OMIM:616145)
Campomelia, Cumming type (Orphanet:1318)
Cantrell pentalogy (Orphanet:1335)
Catel-Manzke syndrome (Orphanet:1388)
Fetal akinesia deformation sequence (Orphanet:994)
Greenberg dysplasia (Orphanet:1426)
Hypochondrogenesis (Orphanet:93297)
Lethal multiple pterygium syndrome (Orphanet:33108)
Meckel syndrome, type 2 (OMIM:603194)
Mosaic trisomy 9 (Orphanet:99776)
NOONAN SYNDROME 1 (OMIM:163950)
Noonan syndrome (Orphanet:648)
Roberts syndrome (Orphanet:3103)
Short-rib thoracic dysplasia 7 with or without polydactyly (OMIM:614091)
Trisomy 13 (Orphanet:3378)
Trisomy 1q (Orphanet:261344)
Turner syndrome (Orphanet:881)
X-linked lethal multiple pterygium syndrome (Orphanet:79447)