Misalignment of teeth

Symptom Information:

Symptom ID: HPO:0000692
Synonyms:
Abnormal dental position [HPO:0000692]
Abnormal teeth spacing [HPO:0000692]
Abnormality of teeth spacing [HPO:0000692]
Malaligned teeth [HPO:0000692]
Malposition of teeth [HPO:0000692]
Malpositioned teeth [HPO:0000692]
Abnormal dental position [OMIM:Abnormal dental position]
Abnormal teeth spacing [OMIM:Abnormal teeth spacing]
Malaligned teeth [OMIM:Malaligned teeth]
Malposition of teeth [OMIM:Malposition of teeth]
Malpositioned teeth [OMIM:Malpositioned teeth]
Quality:
Cross references:
OMIM: "Abnormal dental position" [OMIM:Abnormal dental position]
OMIM: "Abnormal teeth spacing" [OMIM:Abnormal teeth spacing]
OMIM: "Malaligned teeth" [OMIM:Malaligned teeth]
OMIM: "Malposition of teeth" [OMIM:Malposition of teeth]
OMIM: "Malpositioned teeth" [OMIM:Malpositioned teeth]
Is a (Direct Parents):
HPO         Abnormality of the 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)
                         Misalignment of teeth(HPO:0000692)
MedDRA:
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

Cataract - intellectual deficit - hypogonadism (Orphanet:1387)
Cranioectodermal dysplasia 1 (OMIM:218330)
Craniometaphyseal dysplasia (Orphanet:1522)
Ectodermal dysplasia - blindness (Orphanet:1806)
Florid cemento-osseous dysplasia (Orphanet:83451)
Glaucoma - ectopia - microspherophakia - stiff joints - short stature (Orphanet:2084)
Greenberg dysplasia (Orphanet:1426)
MALPOSITION OF TEETH WITH OR WITHOUT HYPODONTIA/OLIGODONTIA (OMIM:189490)
MICROPHTHALMIA, SYNDROMIC 1 (OMIM:309800)
Metaphyseal chondrodysplasia, Jansen type (Orphanet:33067)
Monosomy 18p (Orphanet:1598)
Mowat-Wilson syndrome (Orphanet:2152)
Mucopolysaccharidosis type 2 (Orphanet:580)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
VAN BOGAERT-HOZAY SYNDROME (OMIM:277150)
WEILL-MARCHESANI SYNDROME 1 (OMIM:277600)
Weill-Marchesani syndrome (Orphanet:3449)
Wilson-Turner syndrome (Orphanet:3459)