Sarcoma

Symptom Information:

Symptom ID: HPO:0100242
Synonyms:
Sarcoma (disorder) [Orphanet:50820]
Malignant neoplasm of soft tissue (disorder) [Orphanet:50820]
Sarcoma, no ICD-O subtype (morphologic abnormality) [Orphanet:50820]
Sarcoma [Orphanet:50820]
Sarcoma [OMIM:Sarcoma]
Sarcoma [MedDRA:10039491]
Sarcoma NOS [MedDRA:10039491]
Quality:
Cross references:
Orphanet:50820 "Sarcoma" [Orphanet:50820]
OMIM: "Sarcoma" [OMIM:Sarcoma]
UMLS:C1261473 "Sarcoma" [Orphanet:50820]
Is a (Direct Parents):
HPO         Soft tissue sarcoma
HPO         Neoplasm by histology
Orphanet Neoplasm
MedDRA Soft tissue sarcomas histology unspecified
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Neoplasm(HPO:0002664)
          Neoplasm by histology(HPO:0011792)
             Sarcoma(HPO:0100242)
MedDRA:
Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104)
    Soft tissue neoplasms malignant and unspecified(MedDRA:10072990)
       Soft tissue sarcomas histology unspecified(MedDRA:10041298)
          Sarcoma(HPO:0100242)
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

Acquired ichthyosis (Orphanet:454)
Aggressive systemic mastocytosis (Orphanet:98850)
Albright hereditary osteodystrophy (Orphanet:665)
Buschke-Ollendorff syndrome (Orphanet:1306)
Carney triad (Orphanet:139411)
Carney-Stratakis syndrome (Orphanet:97286)
Cutaneous mastocytosis (Orphanet:66646)
Enchondromatosis (Orphanet:296)
Familial adenomatous polyposis (Orphanet:733)
Gastrointestinal stromal tumor (Orphanet:44890)
Gorlin syndrome (Orphanet:377)
Interdigitating dendritic cell sarcoma (Orphanet:86900)
LI-FRAUMENI SYNDROME 2 (OMIM:609265)
Large congenital melanocytic nevus (Orphanet:626)
Li-Fraumeni syndrome (Orphanet:524)
Maffucci syndrome (Orphanet:163634)
Mast cell sarcoma (Orphanet:66661)
Mastocytosis (Orphanet:98292)
McCune-Albright syndrome (Orphanet:562)
Melanoma-pancreatic cancer syndrome (Orphanet:51013)
Non-polyposis Turcot syndrome (Orphanet:99817)
Progressive osseous heteroplasia (Orphanet:2762)
RAPADILINO syndrome (Orphanet:3021)
Rothmund-Thomson syndrome (Orphanet:2909)
Rothmund-Thomson syndrome type 2 (Orphanet:221016)
V-RAF MURINE SARCOMA 3611 VIRAL ONCOGENE HOMOLOG 1 (OMIM:311010)
Werner syndrome (Orphanet:902)