Dental crowding
Symptom Information:
Symptom ID: | HPO:0000678 | |||||||||||||||||||
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 crowding(HPO:0000678) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Dental and gingival conditions(MedDRA:10044018) Dental disorders NEC(MedDRA:10044037) Dental crowding(HPO:0000678) |
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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) |