Macrodontia of permanent maxillary central incisor

Symptom Information:

Symptom ID: HPO:0000675
Synonyms:
Long maxillary central incisors [HPO:0000675]
Prominent upper incisors [HPO:0000675]
Prominent, protruding upper incisors [HPO:0000675]
Long maxillary central incisors [OMIM:Long maxillary central incisors]
Prominent upper incisors [OMIM:Prominent upper incisors]
Prominent, protruding upper incisors [OMIM:Prominent, protruding upper incisors]
Quality:
Cross references:
OMIM: "Long maxillary central incisors" [OMIM:Long maxillary central incisors]
OMIM: "Prominent upper incisors" [OMIM:Prominent upper incisors]
OMIM: "Prominent, protruding upper incisors" [OMIM:Prominent, protruding upper incisors]
Is a (Direct Parents):
HPO         Incisor macrodontia
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 the incisor(HPO:0000676)
                            Abnormality of incisor morphology(HPO:0011063)
                               Incisor macrodontia(HPO:0011081)
                                  Macrodontia of permanent maxillary central incisor(HPO:0000675)
                         Abnormality of dental morphology(HPO:0006482)
                            Abnormality of incisor morphology(HPO:0011063)
                               Incisor macrodontia(HPO:0011081)
                                  Macrodontia of permanent maxillary central incisor(HPO:0000675)
                            Macrodontia(HPO:0001572)
                               Incisor macrodontia(HPO:0011081)
                                  Macrodontia of permanent maxillary central incisor(HPO:0000675)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

CEREBELLOFACIODENTAL SYNDROME (OMIM:616202)
Cohen syndrome (Orphanet:193)
INCISORS, LONG UPPER CENTRAL (OMIM:147300)
Macrocephaly - spastic paraplegia - dysmorphism (Orphanet:2429)
Marshall syndrome (Orphanet:560)
OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:257850)
Pachygyria - epilepsy - intellectual deficit - dysmorphism (Orphanet:94084)