Gingival fibromatosis
Symptom Information:
Symptom ID: | HPO:0000169 | |||||||||||
Synonyms: |
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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) Fibrous tissue neoplasm(HPO:0012316) Fibroma(HPO:0010614) Gingival fibromatosis(HPO:0000169) Abnormality of head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormality of the mouth(HPO:0000153) Abnormality of the oral cavity(HPO:0000163) Abnormality of the gingiva(HPO:0000168) Gingival fibromatosis(HPO:0000169) MedDRA: |
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Database Frequency: | 14 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
Amelogenesis imperfecta and gingival hyperplasia syndrome | (Orphanet:171836) |
Desmosterolosis | (Orphanet:35107) |
FIBROMATOSIS, GINGIVAL, 1 | (OMIM:135300) |
Gingival fibromatosis - facial dysmorphism | (Orphanet:2025) |
Gingival fibromatosis - progressive deafness | (Orphanet:2027) |
Gingival fibromatosis-hypertrichosis syndrome | (Orphanet:2026) |
Hereditary gingival fibromatosis | (Orphanet:2024) |
Juvenile hyaline fibromatosis | (Orphanet:2028) |
MELAS | (Orphanet:550) |
Ramon syndrome | (Orphanet:3019) |
TUBEROUS SCLEROSIS 1 | (OMIM:191100) |
TUBEROUS SCLEROSIS 2 | (OMIM:613254) |
Tuberous sclerosis | (Orphanet:805) |
Zimmermann-Laband syndrome | (Orphanet:3473) |