Gingival overgrowth
Symptom Information:
Symptom ID: | HPO:0000212 | ||||||||||||||
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) 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 overgrowth(HPO:0000212) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Dental and gingival conditions(MedDRA:10044018) Gingival disorders NEC(MedDRA:10018776) Gingival overgrowth(HPO:0000212) |
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Database Frequency: | 43 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
Alpha-mannosidosis | (Orphanet:61) |
Amelogenesis imperfecta - nephrocalcinosis | (Orphanet:1031) |
Amelogenesis imperfecta and gingival hyperplasia syndrome | (Orphanet:171836) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Cleft palate | (Orphanet:2014) |
Dermato-cardio-skeletal syndrome, Borrone type | (Orphanet:1266) |
Dermochondrocorneal dystrophy | (Orphanet:79149) |
Ehlers-Danlos syndrome, dermatosparaxis type | (Orphanet:1901) |
FGFR2-related bent bone dysplasia | (Orphanet:313855) |
Frank-Ter Haar syndrome | (Orphanet:137834) |
Free sialic acid storage disease, infantile form | (Orphanet:309324) |
Fucosidosis | (Orphanet:349) |
GM1 gangliosidosis | (Orphanet:354) |
GM1 gangliosidosis type 1 | (Orphanet:79255) |
HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVEFACIAL FEATURES | (OMIM:609943) |
Hennekam syndrome | (Orphanet:2136) |
Hurler syndrome | (Orphanet:93473) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Hypoplasminogenemia | (Orphanet:722) |
Juvenile hyaline fibromatosis | (Orphanet:2028) |
Lathosterolosis | (Orphanet:46059) |
Leprechaunism | (Orphanet:508) |
Lethal osteosclerotic bone dysplasia | (Orphanet:1832) |
Ligneous conjunctivitis | (Orphanet:97231) |
MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY | (OMIM:606369) |
MACS syndrome | (Orphanet:217335) |
MELAS | (Orphanet:550) |
MGAT2-CDG | (Orphanet:79329) |
Marshall-Smith syndrome | (Orphanet:561) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 | (Orphanet:300496) |
Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 | (OMIM:600462) |
PELGER-HUET ANOMALY | (OMIM:169400) |
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2 | (OMIM:616331) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Recombinant 8 syndrome | (Orphanet:96167) |
TMCO1 defect syndrome | (Orphanet:228407) |
Torg-Winchester syndrome | (Orphanet:3460) |
WINCHESTER SYNDROME | (OMIM:277950) |
Zimmermann-Laband syndrome | (Orphanet:3473) |