Dental malocclusion

Symptom Information:

Symptom ID: HPO:0000689
Synonyms:
Malocclusion [HPO:0000689]
Malocclusion of teeth (disorder) [Orphanet:3760]
Malocclusion [Orphanet:3760]
Dental malocclusion [OMIM:Dental malocclusion]
Malocclusion [OMIM:Malocclusion]
Dental malocclusion [Orphanet:3760]
Malocclusion [MedDRA:10061274]
Malocclusion NOS [MedDRA:10061274]
Malocclusion, unspecified [MedDRA:10061274]
Underbite [MedDRA:10061274]
Overbite [MedDRA:10061274]
Malocclusion (in some patients) [OMIM:Malocclusion (in some patients)]
Quality:
Cross references:
HPO:0010807 "Open bite" [Orphanet:3760]
Orphanet:3760 "Dental malocclusion" [Orphanet:3760]
OMIM: "Dental malocclusion" [OMIM:Dental malocclusion]
OMIM: "Malocclusion" [OMIM:Malocclusion]
OMIM: "Malocclusion (in some patients)" [OMIM:Malocclusion (in some patients)]
UMLS:C0024636 "Malocclusion" [Orphanet:3760]
Is a (Direct Parents):
HPO         Misalignment of teeth
MedDRA Dental disorders NEC
Orphanet Abnormal facial shape
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)
                            Dental malocclusion(HPO:0000689)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Dental and gingival conditions(MedDRA:10044018)
       Dental disorders NEC(MedDRA:10044037)
          Dental malocclusion(HPO:0000689)
Database Frequency: 114 / 7739
Resource:

All diseases associated with this symptom:

17p11.2 microduplication syndrome (Orphanet:1713)
48,XXXY syndrome (Orphanet:96263)
48,XXYY syndrome (Orphanet:10)
49,XXXXY syndrome (Orphanet:96264)
ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE (OMIM:101800)
AURICULOCONDYLAR SYNDROME 1 (OMIM:602483)
AURICULOCONDYLAR SYNDROME 2 (OMIM:614669)
Acro-oto-ocular syndrome (Orphanet:2980)
Acrodysostosis (Orphanet:950)
Acrodysostosis with multiple hormone resistance (Orphanet:280651)
Acroosteolysis, dominant type (Orphanet:955)
Alpha-mannosidosis (Orphanet:61)
Aneurysm - osteoarthritis syndrome (Orphanet:284984)
Apert syndrome (Orphanet:87)
Auriculocondylar syndrome (Orphanet:137888)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal dominant osteosclerosis, Worth type (Orphanet:2790)
Autosomal dominant prognathism (Orphanet:2964)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 2 (OMIM:615981)
Bardet-Biedl syndrome 4 (OMIM:615982)
Bencze syndrome (Orphanet:1241)
Bird headed-dwarfism, Montreal type (Orphanet:2617)
CARDIOFACIOCUTANEOUS SYNDROME 1 (OMIM:115150)
CEREBELLOFACIODENTAL SYNDROME (OMIM:616202)
CHARGE syndrome (Orphanet:138)
COCKAYNE SYNDROME A (OMIM:216400)
COCKAYNE SYNDROME B (OMIM:133540)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Cerebro-facio-articular syndrome (Orphanet:314679)
Cleidocranial dysplasia (Orphanet:1452)
Cockayne syndrome (Orphanet:191)
Coffin-Lowry syndrome (Orphanet:192)
Craniofacial dysplasia-osteopenia syndrome (Orphanet:314555)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Craniosynostosis - fibular aplasia (Orphanet:1533)
Deafness - intellectual deficit, Martin-Probst type (Orphanet:85321)
Developmental delay-microcephaly-facial dysmorphism syndrome, Hutterite type (Orphanet:363444)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, spondylocheirodysplastic type (Orphanet:157965)
FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES,AND SPONTANEOUS FILTERING BLEBS (OMIM:601552)
FACIOCARDIOMELIC SYNDROME (OMIM:612731)
Familial scaphocephaly syndrome, McGillivray type (Orphanet:168624)
Focal dermal hypoplasia (Orphanet:2092)
Frank-Ter Haar syndrome (Orphanet:137834)
Fraser syndrome (Orphanet:2052)
Frontometaphyseal dysplasia (Orphanet:1826)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
Grant syndrome (Orphanet:2097)
HAJDU-CHENEY SYNDROME (OMIM:102500)
HOLOPROSENCEPHALY 7 (OMIM:610828)
HOLOPROSENCEPHALY 9 (OMIM:610829)
Hallermann-Streiff syndrome (Orphanet:2108)
Harrod syndrome (Orphanet:2115)
Hemifacial hypertrophy (Orphanet:141145)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Hypocalcified amelogenesis imperfecta (Orphanet:100032)
Hypospadias - hypertelorism - coloboma and deafness (Orphanet:157788)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Intellectual deficit, X-linked, Vitale type (Orphanet:85289)
KABUKI SYNDROME 2 (OMIM:300867)
Larsen-like osseous dysplasia - short stature (Orphanet:2370)
MALOCCLUSION DUE TO PROTUBERANT UPPER FRONT TEETH (OMIM:154300)
MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT (OMIM:608257)
MOMO syndrome (Orphanet:2563)
MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY (OMIM:608931)
Marfan syndrome (Orphanet:558)
Maxillo-nasal dysplasia (Orphanet:1248)
McCune-Albright syndrome (Orphanet:562)
McDonough syndrome (Orphanet:2471)
Monosomy 22q13 (Orphanet:48652)
NOONAN SYNDROME 1 (OMIM:163950)
NOONAN SYNDROME 4 (OMIM:610733)
Noonan syndrome (Orphanet:648)
OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:257850)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3 (OMIM:259730)
OTOFACIOCERVICAL SYNDROME 2 (OMIM:615560)
Oculocerebrorenal syndrome (Orphanet:534)
Oculofaciocardiodental syndrome (Orphanet:2712)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Odonto-tricho-ungual-digito-palmar syndrome (Orphanet:69082)
Oliver syndrome (Orphanet:2920)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Osteopetrosis with renal tubular acidosis (Orphanet:2785)
Otodental syndrome (Orphanet:2791)
Peters anomaly (Orphanet:708)
Progressive hemifacial atrophy (Orphanet:1214)
Proteus-like syndrome (Orphanet:2969)
Pyle disease (Orphanet:3005)
RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME (OMIM:616108)
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2 (OMIM:616331)
Rabson-Mendenhall syndrome (Orphanet:769)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency (Orphanet:353284)
SCLEROSTEOSIS 1 (OMIM:269500)
SHORT syndrome (Orphanet:3163)
Sclerosteosis (Orphanet:3152)
Seckel syndrome (Orphanet:808)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Spondylometaphyseal dysplasia - cone-rod dystrophy (Orphanet:85167)
Stickler syndrome (Orphanet:828)
TRICHORHINOPHALANGEAL SYNDROME, TYPE I (OMIM:190350)
Tel Hashomer camptodactyly syndrome (Orphanet:3292)
Treacher-Collins syndrome (Orphanet:861)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
VAN MALDERGEM SYNDROME 1 (OMIM:601390)
VAN MALDERGEM SYNDROME 2 (OMIM:615546)
Williams syndrome (Orphanet:904)