Delayed eruption of permanent teeth

Symptom Information:

Symptom ID: HPO:0000696
Synonyms:
Delayed eruption of secondary teeth [HPO:0000696]
Delayed permanent dentition [HPO:0000696]
Delayed eruption of permanent teeth [OMIM:Delayed eruption of permanent teeth]
Delayed eruption of secondary teeth [OMIM:Delayed eruption of secondary teeth]
Delayed permanent dentition [OMIM:Delayed permanent dentition]
Delayed eruption of permanent teeth (rare) [OMIM:Delayed eruption of permanent teeth (rare)]
Quality:
Cross references:
OMIM: "Delayed eruption of permanent teeth" [OMIM:Delayed eruption of permanent teeth]
OMIM: "Delayed eruption of secondary teeth" [OMIM:Delayed eruption of secondary teeth]
OMIM: "Delayed permanent dentition" [OMIM:Delayed permanent dentition]
OMIM: "Delayed eruption of permanent teeth (rare)" [OMIM:Delayed eruption of permanent teeth (rare)]
Is a (Direct Parents):
HPO         Delayed eruption of 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 dental eruption(HPO:0006292)
                            Delayed eruption of teeth(HPO:0000684)
                               Delayed eruption of permanent teeth(HPO:0000696)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Amelogenesis imperfecta - nephrocalcinosis (Orphanet:1031)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Brachydactyly type B (Orphanet:93383)
CLEIDOCRANIAL DYSPLASIA (OMIM:119600)
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:218400)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Cleidocranial dysplasia (Orphanet:1452)
Gingival fibromatosis - facial dysmorphism (Orphanet:2025)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 15 (OMIM:614608)
Pycnodysostosis (Orphanet:763)
SENER SYNDROME (OMIM:606156)
Weismann-Netter syndrome (Orphanet:3344)