Delayed eruption of primary teeth

Symptom Information:

Symptom ID: HPO:0000680
Synonyms:
Delayed eruption of deciduous teeth [HPO:0000680]
Delayed primary teeth eruption [HPO:0000680]
Delayed eruption of deciduous teeth [OMIM:Delayed eruption of deciduous teeth]
Delayed eruption of primary teeth [OMIM:Delayed eruption of primary teeth]
Delayed primary teeth eruption [OMIM:Delayed primary teeth eruption]
Quality:
Cross references:
OMIM: "Delayed eruption of deciduous teeth" [OMIM:Delayed eruption of deciduous teeth]
OMIM: "Delayed eruption of primary teeth" [OMIM:Delayed eruption of primary teeth]
OMIM: "Delayed primary teeth eruption" [OMIM:Delayed primary teeth eruption]
Is a (Direct Parents):
HPO         Delayed eruption of teeth
HPO         Abnormality of primary teeth
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 primary teeth(HPO:0006481)
                            Delayed eruption of primary teeth(HPO:0000680)
                         Abnormality of dental eruption(HPO:0006292)
                            Delayed eruption of teeth(HPO:0000684)
                               Delayed eruption of primary teeth(HPO:0000680)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

CLEIDOCRANIAL DYSPLASIA (OMIM:119600)
COCKAYNE SYNDROME A (OMIM:216400)
COCKAYNE SYNDROME B (OMIM:133540)
Cleidocranial dysplasia (Orphanet:1452)
Cockayne syndrome (Orphanet:191)
Emanuel syndrome (Orphanet:96170)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Non-eruption of teeth - maxillary hypoplasia - genu valgum (Orphanet:2972)
Oculodental syndrome, Rutherfurd type (Orphanet:2709)
Pycnodysostosis (Orphanet:763)