Embryonal neoplasm
Symptom Information:
Symptom ID: | HPO:0002898 | |||
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 histology(HPO:0011792) Embryonal neoplasm(HPO:0002898) MedDRA: |
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Database Frequency: | 6 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Beckwith-Wiedemann syndrome due to CDKN1C mutation | (Orphanet:231120) |
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 | (Orphanet:231117) |
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 | (Orphanet:96193) |
Hemihypertrophy | (Orphanet:2128) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |