Gingival overgrowth

Symptom Information:

Symptom ID: HPO:0000212
Synonyms:
Gingival hyperplasia [HPO:0000212]
Gingival hypertrophy [HPO:0000212]
Gum hypertrophy [HPO:0000212]
Gingival enlargement (disorder) [Orphanet:10770]
Gingival Overgrowth [Orphanet:10770]
Gingival hyperplasia [OMIM:Gingival hyperplasia]
Gingival hypertrophy [OMIM:Gingival hypertrophy]
Gingival overgrowth [OMIM:Gingival overgrowth]
Gum hypertrophy [OMIM:Gum hypertrophy]
Thickened/hypertrophic/fibromatous gingivae [Orphanet:10770]
Gingival hyperplasia (36%) [OMIM:Gingival hyperplasia (36%)]
Gingival hyperplasia (71%) [OMIM:Gingival hyperplasia (71%)]
Gingival hyperplasia [MedDRA:10018283]
Gingival hypertrophy [MedDRA:10018284]
Quality:
Cross references:
Orphanet:10770 "Thickened/hypertrophic/fibromatous gingivae" [Orphanet:10770]
OMIM: "Gingival hyperplasia" [OMIM:Gingival hyperplasia]
OMIM: "Gingival hypertrophy" [OMIM:Gingival hypertrophy]
OMIM: "Gingival overgrowth" [OMIM:Gingival overgrowth]
OMIM: "Gum hypertrophy" [OMIM:Gum hypertrophy]
OMIM: "Gingival hyperplasia (36%)" [OMIM:Gingival hyperplasia (36%)]
OMIM: "Gingival hyperplasia (71%)" [OMIM:Gingival hyperplasia (71%)]
UMLS:C0376480 "Gingival Overgrowth" [Orphanet:10770]
Is a (Direct Parents):
Orphanet Gingival fibromatosis
HPO         Abnormality of the gingiva
Orphanet Abnormality of the tongue
MedDRA Gingival disorders NEC
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)
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)