Persistence of primary teeth

Symptom Information:

Symptom ID: HPO:0006335
Synonyms:
Deciduous teeth retention [HPO:0006335]
Delayed loss of primary teeth [HPO:0006335]
Persistence of deciduous teeth [HPO:0006335]
Persistent primary dentition [HPO:0006335]
Persistent primary teeth [HPO:0006335]
Retained deciduous teeth [HPO:0006335]
Deciduous teeth retention [OMIM:Deciduous teeth retention]
Delayed loss of primary teeth [OMIM:Delayed loss of primary teeth]
Persistence of deciduous teeth [OMIM:Persistence of deciduous teeth]
Persistent primary teeth [OMIM:Persistent primary teeth]
Retained deciduous teeth [OMIM:Retained deciduous teeth]
Retained deciduous tooth [MedDRA:10070573]
Quality:
Cross references:
OMIM: "Deciduous teeth retention" [OMIM:Deciduous teeth retention]
OMIM: "Delayed loss of primary teeth" [OMIM:Delayed loss of primary teeth]
OMIM: "Persistence of deciduous teeth" [OMIM:Persistence of deciduous teeth]
OMIM: "Persistent primary teeth" [OMIM:Persistent primary teeth]
OMIM: "Retained deciduous teeth" [OMIM:Retained deciduous teeth]
Is a (Direct Parents):
HPO         Abnormality of primary teeth
MedDRA Dental disorders NEC
HPO         Abnormality of dental eruption
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 teeth(HPO:0000164)
                         Abnormality of dental eruption(HPO:0006292)
                            Persistence of primary teeth(HPO:0006335)
                         Abnormality of primary teeth(HPO:0006481)
                            Persistence of primary teeth(HPO:0006335)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Dental and gingival conditions(MedDRA:10044018)
       Dental disorders NEC(MedDRA:10044037)
          Persistence of primary teeth(HPO:0006335)
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Arterial calcification, generalized, of infancy, 1 (OMIM:208000)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Carpenter syndrome (Orphanet:65759)
FAILURE OF TOOTH ERUPTION, PRIMARY (OMIM:125350)
Frontometaphyseal dysplasia (Orphanet:1826)
Gingival fibromatosis - facial dysmorphism (Orphanet:2025)
Kleefstra syndrome (Orphanet:261494)
MELAS (Orphanet:550)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2 (OMIM:259710)
Oculofaciocardiodental syndrome (Orphanet:2712)
Pycnodysostosis (Orphanet:763)