Rhabdomyosarcoma
Symptom Information:
Symptom ID: | HPO:0002859 | ||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Neoplasm(HPO:0002664) Neoplasm by anatomical site(HPO:0011793) Neoplasm of striated muscle(HPO:0009728) Rhabdomyosarcoma(HPO:0002859) Neoplasm by histology(HPO:0011792) Sarcoma(HPO:0100242) Rhabdomyosarcoma(HPO:0002859) MedDRA: Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104) Soft tissue neoplasms malignant and unspecified(MedDRA:10072990) Rhabdomyosarcoma(HPO:0002859) |
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Database Frequency: | 10 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 | (Orphanet:231117) |
Constitutional mismatch repair deficiency syndrome | (Orphanet:252202) |
Costello syndrome | (Orphanet:3071) |
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 | (OMIM:257300) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion | (Orphanet:363700) |
Nijmegen breakage syndrome | (Orphanet:647) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
Pleuropulmonary blastoma | (Orphanet:64742) |
Pleuropulmonary blastoma family tumor susceptibility syndrome | (Orphanet:284343) |