Dental crowding

Symptom Information:

Symptom ID: HPO:0000678
Synonyms:
Crowded teeth [HPO:0000678]
Dental overcrowding [HPO:0000678]
Crowding of teeth [HPO:0000678]
Crowding of teeth (disorder) [Orphanet:12400]
Tooth Crowding [Orphanet:12400]
Crowded teeth [OMIM:Crowded teeth]
Dental crowding [OMIM:Dental crowding]
Dental overcrowding [OMIM:Dental overcrowding]
Abnormal dentition/dental position/implantation/unerupted/dental ankylosis [Orphanet:12400]
Tooth crowding [Orphanet:12400]
Tooth crowding [MedDRA:10070074]
Crowded teeth (49%) [OMIM:Crowded teeth (49%)]
Crowded teeth (94%) [OMIM:Crowded teeth (94%)]
Dental crowding (rare) [OMIM:Dental crowding (rare)]
Tooth crowding [OMIM:Tooth crowding]
Tooth ankylosis [MedDRA:10044019]
Dental ankylosis [Orphanet:12400]
Ankylosis of tooth (disorder) [Orphanet:12400]
Tooth Ankylosis [Orphanet:12400]
Quality:
Cross references:
Orphanet:12400 "Abnormal dentition/dental position/implantation/unerupted/dental ankylosis" [Orphanet:12400]
OMIM: "Crowded teeth" [OMIM:Crowded teeth]
OMIM: "Dental crowding" [OMIM:Dental crowding]
OMIM: "Dental overcrowding" [OMIM:Dental overcrowding]
OMIM: "Crowded teeth (49%)" [OMIM:Crowded teeth (49%)]
OMIM: "Crowded teeth (94%)" [OMIM:Crowded teeth (94%)]
OMIM: "Dental crowding (rare)" [OMIM:Dental crowding (rare)]
OMIM: "Tooth crowding" [OMIM:Tooth crowding]
UMLS:C0040433 "Tooth Crowding" [Orphanet:12400]
UMLS:C0155930 "Tooth Ankylosis" [Orphanet:12400]
Is a (Direct Parents):
HPO         Misalignment of teeth
Orphanet Abnormality of the teeth
MedDRA Dental disorders NEC
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 crowding(HPO:0000678)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Dental and gingival conditions(MedDRA:10044018)
       Dental disorders NEC(MedDRA:10044037)
          Dental crowding(HPO:0000678)
Database Frequency: 65 / 7739
Resource:

All diseases associated with this symptom:

17p11.2 microduplication syndrome (Orphanet:1713)
2q32q33 microdeletion syndrome (Orphanet:251019)
3MC SYNDROME 1 (OMIM:257920)
ASYMMETRIC SHORT STATURE SYNDROME (OMIM:108450)
AURICULOCONDYLAR SYNDROME 1 (OMIM:602483)
AURICULOCONDYLAR SYNDROME 2 (OMIM:614669)
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 (Orphanet:98791)
Auriculocondylar syndrome (Orphanet:137888)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive spastic paraplegia type 49 (Orphanet:320385)
BARATELA-SCOTT SYNDROME (OMIM:300881)
Bangstad syndrome (Orphanet:1227)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 17 (OMIM:615994)
Bardet-Biedl syndrome 2 (OMIM:615981)
Bardet-Biedl syndrome 4 (OMIM:615982)
Bardet-Biedl syndrome 7 (OMIM:615984)
Buschke-Ollendorff syndrome (Orphanet:1306)
CK syndrome (Orphanet:251383)
CRANIOMETADIAPHYSEAL DYSPLASIA (OMIM:269300)
Classical homocystinuria (Orphanet:394)
Craniometadiaphyseal dysplasia, wormian bone type (Orphanet:85184)
Crouzon disease (Orphanet:207)
Distal monosomy 6p (Orphanet:96125)
ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY (OMIM:600906)
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 2 (OMIM:615539)
ENAMEL HYPOPLASIA, CATARACTS, AND AQUEDUCTAL STENOSIS (OMIM:600907)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
Emanuel syndrome (Orphanet:96170)
Fraser syndrome (Orphanet:2052)
Intellectual deficit, X-linked, Snyder type (Orphanet:3063)
LUJAN-FRYNS SYNDROME (OMIM:309520)
Lateral meningocele syndrome (Orphanet:2789)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 23 (OMIM:615761)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 29 (OMIM:616078)
MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES (OMIM:606772)
MENTAL RETARDATION, X-LINKED 19 (OMIM:300844)
MENTAL RETARDATION, X-LINKED 21 (OMIM:300143)
MICROPHTHALMIA, SYNDROMIC 1 (OMIM:309800)
Mandibular hypoplasia-deafness-progeroid syndrome (Orphanet:363649)
Mandibuloacral dysplasia (Orphanet:2457)
Mandibuloacral dysplasia with type A lipodystrophy (Orphanet:90153)
Mandibuloacral dysplasia with type B lipodystrophy (Orphanet:90154)
Marfan syndrome type 1 (Orphanet:284963)
Mulibrey nanism (Orphanet:2576)
Nestor-Guillermo progeria syndrome (Orphanet:280576)
OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:257850)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Pfeiffer syndrome (Orphanet:710)
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2 (OMIM:616331)
Rabson-Mendenhall syndrome (Orphanet:769)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
Ruvalcaba syndrome (Orphanet:3121)
SECKEL SYNDROME 1 (OMIM:210600)
STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES (OMIM:612948)
Sakati-Nyhan syndrome (Orphanet:3128)
Seckel syndrome (Orphanet:808)
Smith-Lemli-Opitz syndrome (Orphanet:818)
TRICHORHINOPHALANGEAL SYNDROME, TYPE III (OMIM:190351)
Temtamy syndrome (Orphanet:1777)
Van den Ende-Gupta syndrome (Orphanet:2460)