Dental malocclusion
Symptom Information:
Symptom ID: | HPO:0000689 | ||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |