Delayed eruption of teeth
Symptom Information:
Symptom ID: | HPO:0000684 | |||||||||||||||||||||
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) Abnormality of dental eruption(HPO:0006292) Delayed eruption of teeth(HPO:0000684) MedDRA: |
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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) |