Abnormality of the gingiva

Symptom Information:

Symptom ID: HPO:0000168
Gingival abnormality [HPO:0000168]
Gingiva anomaly [Orphanet:10000]
Anomalies of tongue, gingiva and oral mucosa [Orphanet:10000]
Cross references:
Orphanet:10000 "Anomalies of tongue, gingiva and oral mucosa" [Orphanet:10000]
Is a (Direct Parents):
HPO         Abnormality of the oral cavity
HPO         Gingival cleft
Orphanet Abnormality of the tongue
Is a (Whole tree): HPO:
    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)
Database Frequency: 51 / 7739

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)
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)