Abnormality of dental morphology

Symptom Information:

Symptom ID: HPO:0006482
Synonyms:
Abnormally shaped teeth [HPO:0006482]
Malformed teeth [HPO:0006482]
Misshapen teeth [HPO:0006482]
Misshapened teeth [HPO:0006482]
Tooth shape anomaly [Orphanet:12050]
Abnormally shaped teeth [OMIM:Abnormally shaped teeth]
Malformed teeth [OMIM:Malformed teeth]
Misshapen teeth [OMIM:Misshapen teeth]
Misshapen teeth (in some patients) [OMIM:Misshapen teeth (in some patients)]
Quality:
Cross references:
Orphanet:12050 "Tooth shape anomaly" [Orphanet:12050]
OMIM: "Abnormally shaped teeth" [OMIM:Abnormally shaped teeth]
OMIM: "Malformed teeth" [OMIM:Malformed teeth]
OMIM: "Misshapen teeth" [OMIM:Misshapen teeth]
OMIM: "Misshapen teeth (in some patients)" [OMIM:Misshapen teeth (in some patients)]
Is a (Direct Parents):
HPO         Abnormality of the teeth
Orphanet 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)
                         Abnormality of dental morphology(HPO:0006482)
MedDRA:
Database Frequency: 81 / 7739
Resource:

All diseases associated with this symptom:

17p11.2 microduplication syndrome (Orphanet:1713)
2q32q33 microdeletion syndrome (Orphanet:251019)
8q22.1 microdeletion syndrome (Orphanet:178303)
ADULT syndrome (Orphanet:978)
Abruzzo-Erickson syndrome (Orphanet:921)
Ackerman syndrome (Orphanet:2561)
Acro-oto-ocular syndrome (Orphanet:2980)
Acrofacial dysostosis, Weyers type (Orphanet:952)
Amelo-onycho-hypohidrotic syndrome (Orphanet:1028)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Atypical dentin dysplasia due to SMOC2 deficiency (Orphanet:314721)
Autosomal dominant hypohidrotic ectodermal dysplasia (Orphanet:1810)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive hypohidrotic ectodermal dysplasia (Orphanet:248)
Blepharo-cheilo-odontic syndrome (Orphanet:1997)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
Blepharoptosis - cleft palate - ectrodactyly - dental anomalies (Orphanet:1258)
CODAS syndrome (Orphanet:1458)
Cherubism (Orphanet:184)
Coffin-Lowry syndrome (Orphanet:192)
Deafness - onychodystrophy (Orphanet:3231)
Deafness with labyrinthine aplasia, microtia, and microdontia (Orphanet:90024)
Dentin dysplasia (Orphanet:1653)
Distal monosomy 6p (Orphanet:96125)
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT (OMIM:129490)
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALRECESSIVE (OMIM:224900)
EEM syndrome (Orphanet:1897)
Ectodermal dysplasia syndrome (Orphanet:79373)
Ectodermal dysplasia, tricho-odonto-onychial type (Orphanet:1818)
Focal dermal hypoplasia (Orphanet:2092)
Fried's tooth and nail syndrome (Orphanet:99672)
Frontometaphyseal dysplasia (Orphanet:1826)
Frontonasal dysplasia with alopecia and genital anomaly (Orphanet:228390)
Fukuda-Miyanomae-Nakata syndrome (Orphanet:2060)
Gingival fibromatosis - facial dysmorphism (Orphanet:2025)
Glaucoma - ectopia - microspherophakia - stiff joints - short stature (Orphanet:2084)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
Hennekam syndrome (Orphanet:2136)
Hurler-Scheie syndrome (Orphanet:93476)
Hypodontia - dysplasia of nails (Orphanet:2228)
Hypohidrotic ectodermal dysplasia (Orphanet:238468)
Incontinentia pigmenti (Orphanet:464)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Ito hypomelanosis (Orphanet:435)
Kabuki syndrome (Orphanet:2322)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Linear nevus sebaceus syndrome (Orphanet:2612)
Microcephaly - cervical spine fusion anomalies (Orphanet:2522)
Microphthalmia, Lenz type (Orphanet:568)
Mikati-Najjar-Sahli syndrome (Orphanet:2558)
Non-eruption of teeth - maxillary hypoplasia - genu valgum (Orphanet:2972)
OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:257850)
Oculotrichodysplasia (Orphanet:2718)
Odonto-onycho dysplasia - alopecia (Orphanet:2722)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Odontotrichomelic syndrome (Orphanet:2723)
Oligodontia (Orphanet:99798)
Osteopetrosis with renal tubular acidosis (Orphanet:2785)
Otodental syndrome (Orphanet:2791)
Phocomelia - ectrodactyly - deafness - sinus arrhythmia (Orphanet:2878)
Pilodental dysplasia - refractive errors (Orphanet:2892)
Polyvalvular heart disease syndrome (Orphanet:228410)
Pycnodysostosis (Orphanet:763)
Renal-genital-middle ear anomalies (Orphanet:1092)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Stoll-Alembik-Finck syndrome (Orphanet:3200)
Syndromic X-linked intellectual deficit 7 (Orphanet:85274)
Tel Hashomer camptodactyly syndrome (Orphanet:3292)
Thumb deformity - alopecia - pigmentation anomaly (Orphanet:2251)
Treacher-Collins syndrome (Orphanet:861)
Tricho-dento-osseous syndrome (Orphanet:3352)
Trichodermodysplasia - dental alterations (Orphanet:3353)
Ulna metaphyseal dysplasia syndrome (Orphanet:1837)
Van den Ende-Gupta syndrome (Orphanet:2460)
WEILL-MARCHESANI SYNDROME 1 (OMIM:277600)
Weaver-Williams syndrome (Orphanet:3448)
Weill-Marchesani syndrome (Orphanet:3449)
Williams syndrome (Orphanet:904)
Wrinkly skin syndrome (Orphanet:2834)
Zlotogora-Ogur syndrome (Orphanet:3253)
Zunich-Kaye syndrome (Orphanet:3474)