Delayed eruption of teeth

Symptom Information:

Symptom ID: HPO:0000684
Synonyms:
Delayed dental development [HPO:0000684]
Delayed dental eruption [HPO:0000684]
Delayed eruption [HPO:0000684]
Delayed teeth eruption [HPO:0000684]
Delayed tooth eruption [HPO:0000684]
Eruption, delayed [HPO:0000684]
Late eruption of teeth [HPO:0000684]
Late tooth eruption [HPO:0000684]
Delayed tooth eruption [Orphanet:12800]
Late tooth eruption (disorder) [Orphanet:12800]
Late tooth eruption [Orphanet:12800]
Delayed dental development [OMIM:Delayed dental development]
Delayed dental eruption [OMIM:Delayed dental eruption]
Delayed eruption [OMIM:Delayed eruption]
Delayed eruption of teeth [OMIM:Delayed eruption of teeth]
Delayed teeth eruption [OMIM:Delayed teeth eruption]
Delayed tooth eruption [OMIM:Delayed tooth eruption]
Late eruption of teeth [OMIM:Late eruption of teeth]
Late tooth eruption [OMIM:Late tooth eruption]
Delayed dentition/eruption of teeth/lack of eruption of teeth [Orphanet:12800]
Delayed eruption (rare) [OMIM:Delayed eruption (rare)]
Quality:
Cross references:
Orphanet:12800 "Delayed dentition/eruption of teeth/lack of eruption of teeth" [Orphanet:12800]
OMIM: "Delayed dental development" [OMIM:Delayed dental development]
OMIM: "Delayed dental eruption" [OMIM:Delayed dental eruption]
OMIM: "Delayed eruption" [OMIM:Delayed eruption]
OMIM: "Delayed eruption of teeth" [OMIM:Delayed eruption of teeth]
OMIM: "Delayed teeth eruption" [OMIM:Delayed teeth eruption]
OMIM: "Delayed tooth eruption" [OMIM:Delayed tooth eruption]
OMIM: "Late eruption of teeth" [OMIM:Late eruption of teeth]
OMIM: "Late tooth eruption" [OMIM:Late tooth eruption]
OMIM: "Delayed eruption (rare)" [OMIM:Delayed eruption (rare)]
UMLS:C0239174 "Late tooth eruption" [Orphanet:12800]
Is a (Direct Parents):
HPO         Abnormality of dental eruption
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 eruption(HPO:0006292)
                            Delayed eruption of teeth(HPO:0000684)
MedDRA:
Database Frequency: 117 / 7739
Resource:

All diseases associated with this symptom:

3M syndrome (Orphanet:2616)
48,XXXY syndrome (Orphanet:96263)
48,XXYY syndrome (Orphanet:10)
49,XXXXY syndrome (Orphanet:96264)
ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE (OMIM:101800)
Aarskog-Scott syndrome (Orphanet:915)
Acro-osteolysis-keloid-like lesions-premature aging syndrome (Orphanet:363665)
Acro-oto-ocular syndrome (Orphanet:2980)
Acrodysostosis (Orphanet:950)
Acrodysostosis with multiple hormone resistance (Orphanet:280651)
Albright hereditary osteodystrophy (Orphanet:665)
Amelo-onycho-hypohidrotic syndrome (Orphanet:1028)
Amelogenesis imperfecta - nephrocalcinosis (Orphanet:1031)
Angel-shaped phalango-epiphyseal dysplasia (Orphanet:63442)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Apert syndrome (Orphanet:87)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
BRACHYDACTYLY, TYPE E2 (OMIM:613382)
Barber-Say syndrome (Orphanet:1231)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
CHARGE syndrome (Orphanet:138)
CHST3-related skeletal dysplasia (Orphanet:263463)
CODAS syndrome (Orphanet:1458)
Camurati-Engelmann disease (Orphanet:1328)
Cleidocranial dysplasia (Orphanet:1452)
Cockayne syndrome (Orphanet:191)
Coffin-Lowry syndrome (Orphanet:192)
Coffin-Siris syndrome (Orphanet:1465)
Cole-Carpenter syndrome (Orphanet:2050)
Cornelia de Lange syndrome (Orphanet:199)
Craniolenticulosutural dysplasia (Orphanet:50814)
Craniosynostosis and dental anomalies (Orphanet:284149)
Deaf blind hypopigmentation syndrome, Yemenite type (Orphanet:3214)
Dentinogenesis imperfecta - short stature - hearing loss - intellectual deficit (Orphanet:71267)
Dermato-cardio-skeletal syndrome, Borrone type (Orphanet:1266)
Dubowitz syndrome (Orphanet:235)
Dysosteosclerosis (Orphanet:1782)
ECTODERMAL DYSPLASIA WITH ADRENAL CYST (OMIM:129550)
Ectodermal dysplasia, Berlin type (Orphanet:1816)
Ehlers-Danlos syndrome, spondylocheirodysplastic type (Orphanet:157965)
Ellis Van Creveld syndrome (Orphanet:289)
Epidermolysis bullosa simplex with anodontia/hypodontia (Orphanet:2325)
Familial adenomatous polyposis (Orphanet:733)
Familial isolated hypoparathyroidism (Orphanet:2238)
Familial isolated hypoparathyroidism due to agenesis of parathyroid gland (Orphanet:2239)
Focal dermal hypoplasia (Orphanet:2092)
Frontometaphyseal dysplasia (Orphanet:1826)
GAPO syndrome (Orphanet:2067)
Genitopatellar syndrome (Orphanet:85201)
Gingival fibromatosis - facial dysmorphism (Orphanet:2025)
Gingival fibromatosis - progressive deafness (Orphanet:2027)
Gingival fibromatosis-hypertrichosis syndrome (Orphanet:2026)
Goldblatt syndrome (Orphanet:166272)
Growth hormone insensitivity syndrome (Orphanet:181393)
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6 (OMIM:614450)
Hall-Riggs syndrome (Orphanet:2107)
Hennekam syndrome (Orphanet:2136)
Hurler syndrome (Orphanet:93473)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
Hydrocephalus - blue sclerae - nephropathy (Orphanet:2186)
Hypertrichosis (Orphanet:79365)
Hypertrichosis lanuginosa congenita (Orphanet:2222)
Hypocalcemic vitamin D-dependent rickets (Orphanet:289157)
Hypocalcemic vitamin D-resistant rickets (Orphanet:93160)
Hypodontia - dysplasia of nails (Orphanet:2228)
Hypophosphatemic rickets (Orphanet:437)
Incontinentia pigmenti (Orphanet:464)
Intellectual deficit - balding - patella luxation - acromicria (Orphanet:3041)
Isolated sulfite oxidase deficiency (Orphanet:99731)
Johanson-Blizzard syndrome (Orphanet:2315)
KID syndrome (Orphanet:477)
Kleefstra syndrome (Orphanet:261494)
LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM (OMIM:614381)
Laron syndrome (Orphanet:633)
Leukocyte adhesion deficiency (Orphanet:2968)
Low birth weight - dwarfism - dysgammaglobulinemia (Orphanet:2621)
Lowry-MacLean syndrome (Orphanet:2409)
MOMO syndrome (Orphanet:2563)
Microphthalmia, Lenz type (Orphanet:568)
Miller-Dieker syndrome (Orphanet:531)
Monosomy 9q22.3 (Orphanet:77301)
Mowat-Wilson syndrome (Orphanet:2152)
Mucopolysaccharidosis type 2 (Orphanet:580)
Non-eruption of teeth - maxillary hypoplasia - genu valgum (Orphanet:2972)
OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:257850)
OSTEOGENESIS IMPERFECTA, TYPE XII (OMIM:613849)
Oculocerebrorenal syndrome (Orphanet:534)
Oculodental syndrome, Rutherfurd type (Orphanet:2709)
Oculofaciocardiodental syndrome (Orphanet:2712)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Otodental syndrome (Orphanet:2791)
Progressive hemifacial atrophy (Orphanet:1214)
Pseudohypoparathyroidism type 1A (Orphanet:79443)
Pseudohypoparathyroidism type 1C (Orphanet:79444)
Pseudopseudohypoparathyroidism (Orphanet:79445)
Pycnodysostosis (Orphanet:763)
Ramon syndrome (Orphanet:3019)
Rothmund-Thomson syndrome (Orphanet:2909)
SHORT syndrome (Orphanet:3163)
Scalp-ear-nipple syndrome (Orphanet:2036)
Short stature - wormian bones - dextrocardia (Orphanet:2863)
Spondyloenchondrodysplasia (Orphanet:1855)
TRICHORHINOPHALANGEAL SYNDROME, TYPE I (OMIM:190350)
Tetrasomy 12p (Orphanet:884)
Torg-Winchester syndrome (Orphanet:3460)
Tricho-dento-osseous syndrome (Orphanet:3352)
Trichodermodysplasia - dental alterations (Orphanet:3353)
Trichomegaly - retina pigmentary degeneration - dwarfism (Orphanet:3363)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A (OMIM:264700)
VITAMIN D-DEPENDENT RICKETS, TYPE 2A (OMIM:277440)
Wrinkly skin syndrome (Orphanet:2834)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
Zimmermann-Laband syndrome (Orphanet:3473)