Abnormality of the gingiva
Symptom Information:
Symptom ID: | HPO:0000168 | ||||||
Synonyms: |
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Quality: | |||||||
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) 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) MedDRA: |
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Database Frequency: | 51 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Acromegaloid facial appearance syndrome | (Orphanet:965) |
Alpha-mannosidosis | (Orphanet:61) |
Amelogenesis imperfecta and gingival hyperplasia syndrome | (Orphanet:171836) |
Aspartylglucosaminuria | (Orphanet:93) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Axial mesodermal dysplasia spectrum | (Orphanet:1834) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
C syndrome | (Orphanet:1308) |
COWDEN SYNDROME 4 | (OMIM:615107) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Cataract - deafness - hypogonadism | (Orphanet:1383) |
Cleft palate - large ears - small head | (Orphanet:2013) |
Cohen syndrome | (Orphanet:193) |
Cowden syndrome | (Orphanet:201) |
Dermato-cardio-skeletal syndrome, Borrone type | (Orphanet:1266) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
Ehlers-Danlos syndrome, periodontitis type | (Orphanet:75392) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Focal palmoplantar and gingival keratoderma | (Orphanet:2200) |
Fountain syndrome | (Orphanet:3219) |
GM1 gangliosidosis | (Orphanet:354) |
Gingival fibromatosis - facial dysmorphism | (Orphanet:2025) |
Gingival fibromatosis - progressive deafness | (Orphanet:2027) |
Gingival fibromatosis-hypertrichosis syndrome | (Orphanet:2026) |
Grix-Blankenship-Peterson syndrome | (Orphanet:2099) |
Haim-Munk syndrome | (Orphanet:2342) |
Hennekam syndrome | (Orphanet:2136) |
Hereditary gingival fibromatosis | (Orphanet:2024) |
Hereditary mucoepithelial dysplasia | (Orphanet:1839) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hypertrichosis | (Orphanet:79365) |
Hypertrichosis lanuginosa congenita | (Orphanet:2222) |
Infantile myofibromatosis | (Orphanet:2591) |
Juvenile hyaline fibromatosis | (Orphanet:2028) |
Lathosterolosis | (Orphanet:46059) |
Lethal osteosclerotic bone dysplasia | (Orphanet:1832) |
Marshall-Smith syndrome | (Orphanet:561) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
Oculodental syndrome, Rutherfurd type | (Orphanet:2709) |
Otodental syndrome | (Orphanet:2791) |
PEHO syndrome | (Orphanet:2836) |
Ramon syndrome | (Orphanet:3019) |
Recombinant 8 syndrome | (Orphanet:96167) |
Scheie syndrome | (Orphanet:93474) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Sturge-Weber syndrome | (Orphanet:3205) |
Torg-Winchester syndrome | (Orphanet:3460) |
Williams syndrome | (Orphanet:904) |
Zimmermann-Laband syndrome | (Orphanet:3473) |