Cystic hygroma
Symptom Information:
Symptom ID: | HPO:0000476 | |||||||||||
Synonyms: |
|
|||||||||||
Quality: | ||||||||||||
Cross references: |
|
|||||||||||
Is a (Direct Parents): |
|
|||||||||||
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) |