Tooth discoloration
Symptom Checker

Results: 80 causes of Tooth discoloration

1. Albuterol - Teratogenic Agent
 There is strong evidence to indicate that exposure to Albuterol during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of ex...read more »
2. Alkaptonuria
 A rare disorder where the abnormal accumulation of a particular acid (homogentisic acid) in the body causes connective tissue and bone damage. This damage gives tissues a dark or bluish discoloration....read more »
3. Amelo-cerebro-hypohidrotic syndrome
 A rare syndrome involving degeneration of the central nervous system, seizures and abnormal tooth development....read more »
4. Amelogenesis imperfecta pigmented hypomaturation type
 Amelogenesis imperfecta is an inherited tooth development disorder characterized by tooth enamel defects. The pigmented hypomaturation type is characterized by fragile tooth enamel which tends to be soft and rough and is usually a creamy to yellow/brown c...read more »
5. Amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 2
 A rare inherited disorder involving abnormal formation of the tooth enamel which causes it to be thin and soft. The abnormality is inherited in a X-linked manner (Xq22-q28)....read more »
6. Autoimmune thyroid disease associated Celiac Disease
 Patients with autoimmune thyroid disease are more susceptible to developing celiac disease than the average population. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of sympto...read more »
7. Basan syndrome
 A rare condition characterized by skin, hair and nail abnormalities....read more »
8. Bulimia nervosa
 Eating disorder with binging (overeating) and purging (vomiting)....read more »
9. Calcium metabolism disorders
10. Celiac Disease
 Digestive intolerance to gluten in the diet....read more »
11. Celiac disease, susceptibility to 1
 The susceptibility to developing celiac disease due to a genetic defect on chromosome 6p21.3. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small int...read more »
12. Celiac disease, susceptibility to 10
 The susceptibility to developing celiac disease due to a genetic defect on chromosome 3q25-q26. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small i...read more »
13. Celiac disease, susceptibility to 11
 The susceptibility to developing celiac disease due to a genetic defect on chromosome 3q28. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intes...read more »
14. Celiac disease, susceptibility to 12
 The susceptibility to developing celiac disease due to a genetic defect on chromosome 6q25.3. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small int...read more »
15. Celiac disease, susceptibility to 13
 The susceptibility to developing celiac disease due to a genetic defect in the SH2B3 gene on chromosome 12q24. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation...read more »
16. Celiac disease, susceptibility to 2
 The susceptibility to developing celiac disease due to a genetic defect on chromosome 5q31-q33. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small i...read more »
17. Celiac disease, susceptibility to 3
 The susceptibility to developing celiac disease due to a genetic defect on chromosome 2q33. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intes...read more »
18. Celiac disease, susceptibility to 4
 The susceptibility to developing celiac disease due to a genetic defect on chromosome 19p13.1. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small in...read more »
19. Celiac disease, susceptibility to 5
 The susceptibility to developing celiac disease due to a genetic defect on chromosome 15q11-q13. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small ...read more »
20. Celiac disease, susceptibility to 6
 The susceptibility to developing celiac disease due to a genetic defect on chromosome 4q27. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intes...read more »
21. Celiac disease, susceptibility to 7
 The susceptibility to developing celiac disease due to a genetic defect on chromosome 1q31. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intes...read more »
22. Celiac disease, susceptibility to 8
 The susceptibility to developing celiac disease due to a genetic defect on chromosome 2q11-q12. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small i...read more »
23. Celiac disease, susceptibility to 9
 The susceptibility to developing celiac disease due to a genetic defect on chromosome 3p21. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intes...read more »
24. Chemical poisoning
 Morbid condition caused by chemical....read more »
25. Chemical poisoning - Selenium
 Selenium is a chemical element used mainly as an industrial catalyst, in glass and ceramic manufacturing, as an animal feed additive, in photography and in the electronics industry. Ingestion and other exposures to the chemical can cause various symptoms....read more »
26. Collagenous celiac disease
 Collagenous celiac disease is used to describe progressive celiac disease characterized by the presence of a layer of collagen (scarring) in the intestinal layers. This form of celiac disease usually fails to respond to treatments such as gluten-free diet...read more »
27. Cone rod dystrophy - amelogenesis imperfecta
 A rare genetic disorder characterized by degeneration of parts of the eye that absorb light (cone rod dystrophy) as well as teeth abnormalities....read more »
28. Demeclocycline - Teratogenic Agent
 There is evidence to indicate that exposure to Demeclocycline (an antibiotic) during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by t...read more »
29. Dental caries
 A destructive process causing decalcification of the tooth enamel leading to cavitation of the tooth...read more »
30. Dentin dysplasia
 A genetic condition characterized by abnormal dentin in primary and/or secondary teeth. Dentin is the calcified structure directly under the outer tooth enamel but surrounding the inner tooth pulp. There are three subtypes of the condition with variable s...read more »
31. Dentin dysplasia, coronal
 A rare inherited disorder characterized by opalescent primary teeth and abnormal secondary teeth which appear normal....read more »
32. Dentinogenesis Imperfecta Type III
 A rare inherited dental disorder where the tops of primary and secondary teeth quickly erode leaving the inside of the tooth exposed....read more »
33. Dentinogenesis imperfecta type Brandywine
 A rare inherited dental disorder where the tops of primary and secondary teeth quickly erode leaving the inside of the tooth exposed....read more »
34. Dentinogenesis imperfecta, type I
 A rare inherited condition which occurs in people suffering from osteogenesis imperfecta (brittle bone disease) and is characterized by tooth structure abnormalities....read more »
35. Dentinogenesis imperfecta, type II
 A rare inherited dental disorder where the tops of primary and secondary teeth quickly erode leaving the inside of the tooth exposed....read more »
36. Down's syndrome associated Celiac Disease
 Patients with Down's syndrome have a high degree of susceptibility to developing celiac disease. Up to 17% of Down's syndrome sufferers develop celiac disease but this rate varies amongst age groups and country of origin. Celiac disease is an autoimmune d...read more »
37. Doxycycline - Teratogenic Agent
 There is evidence to indicate that exposure to Doxycycline during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposur...read more »
38. Engelhard-Yatziv syndrome
 A rare syndrome characterized mainly by droopy eyelids, small head and finger and toe abnormalities....read more »
39. Fluorosis
 Excessive fluoride in the body...read more »
40. Fungal infections
 Any condition caused by fungus....read more »
41. Hutchinson Gilford Syndrome
 A rare genetic disorder characterized by alopecia and senile-like appearance....read more »
42. Hypomelanosis of Ito
 A rare genetic neurocutaneous disorder characterized by unusual patterns of depigmented skin and associated disorders such as seizures, psychomotor retardation and eye abnormalities....read more »
43. Kernicterus
 A rare condition involving high blood levels of bilirubin which can also accumulate in the brain and lead to neurological problems....read more »
44. Kohlschutter-Tonz syndrome
 A rare syndrome involving degeneration of the central nervous system, seizures and abnormal tooth development....read more »
45. Ledermycin - Teratogenic Agent
 There is evidence to indicate that exposure to Ledermycin (an antibiotic) during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the l...read more »
46. Lobstein disease
 A group of rare inherited diseases that involves fragile bones. There are many different types based on the severity and extent of symptoms. Some types are severe enough to cause stillbirth or infant death whereas other types may cause few if any problema...read more »
47. Minocycline - Teratogenic Agent
 There is evidence to indicate that exposure to Minocycline during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposur...read more »
48. Oculodentoosseous dysplasia dominant
 A very rare dominantly inherited syndrome characterized mainly by eye, tooth and finger abnormalities....read more »
49. Osteogenesis imperfecta, type 1A
 A rare genetic connective tissue disorder characterized by fragile bones and hyperextensible joints - a type of osteogenesis imperfecta I where the teeth are opalescent and blue sclerae may be absent....read more »
50. Osteogenesis imperfecta, type 2
 A rare lethal form of the genetic connective tissue disorder characterized by fragile bones, blue sclerae and facial and tooth abnormalities....read more »
51. Osteogenesis imperfecta, type 2A
 A rare lethal form of a genetic connective tissue disorder characterized by fragile bones, blue sclerae and facial and tooth abnormalities. Type IIA has a different origin of the genetic mutation but the clinical features are similar. Type IIA involves a ...read more »
52. Osteogenesis imperfecta, type IIB
 A rare, recessively inherited, lethal form of a genetic connective tissue disorder characterized by fragile bones, blue sclerae and facial and tooth abnormalities. Type IIB has a different origin of the genetic mutation but the clinical features are simil...read more »
53. Porphyria
 A group of disorders characterized by excess production of porphyrin or its precursors which affects the skin and/or nervous system....read more »
54. Psychiatric disorders associated Celiac Disease
 Patients with Psychiatric disorders are more susceptible to developing celiac disease than the average population. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms va...read more »
55. Refractory Celiac Disease
 Refractory Celiac Disease is celiac disease that fails to respond to treatment which involves a gluten-free diet. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The condition is quite uncommon and o...read more »
56. Rickets
 A rare condition where a lack of Vitamin D results in bone disease as it is essential for the process of bone calcification....read more »
57. Smoking
 The smoking of cigarettes...read more »
58. Spira syndrome
 Chronic fluoride intoxication that can occur from flouridated water as well as exposure to vapors or dusts from various industries, agricultures or mines. The main symptoms are teeth anomalies and gastrointestinal symptoms....read more »
59. Stoll-Alembik-Finck syndrome
 A very rare syndrome characterized mainly by muscle, skin, sweating, tooth and facial abnormalities....read more »
60. Susceptibility to Celiac Disease 1
 Susceptibility to celiac disease 1 is a term allocated to a genetic defect on a particular chromosome (chromosome 6p21.3) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly...read more »
61. Susceptibility to Celiac Disease 10
 Susceptibility to celiac disease 10 is a term allocated to a genetic defect on a particular chromosome (chromosome 3q25-q26) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anom...read more »
62. Susceptibility to Celiac Disease 11
 Susceptibility to celiac disease 11 is a term allocated to a genetic defect on a particular chromosome (chromosome 3q28) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly ...read more »
63. Susceptibility to Celiac Disease 12
 Susceptibility to celiac disease 12 is a term allocated to a genetic defect on a particular chromosome (chromosome 6q25) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly ...read more »
64. Susceptibility to Celiac Disease 13
 Susceptibility to celiac disease 13 is a term allocated to a genetic defect on a particular chromosome (chromosome 12q24) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly...read more »
65. Susceptibility to Celiac Disease 2
 Susceptibility to celiac disease 2 is a term allocated to a genetic defect on a particular chromosome (chromosome 5q31-q33) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anoma...read more »
66. Susceptibility to Celiac Disease 3
 Susceptibility to celiac disease 3 is a term allocated to a genetic defect on a particular chromosome (chromosome 2q33) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly d...read more »
67. Susceptibility to Celiac Disease 4
 Susceptibility to celiac disease 4 is a term allocated to a genetic defect on a particular chromosome (chromosome 19p13.1) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomal...read more »
68. Susceptibility to Celiac Disease 5
 Susceptibility to celiac disease 5 is a term allocated to a genetic defect on a particular chromosome (chromosome 15q11-q13) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anom...read more »
69. Susceptibility to Celiac Disease 6
 Susceptibility to celiac disease 6 is a term allocated to a genetic defect on a particular chromosome (chromosome 4q27) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly d...read more »
70. Susceptibility to Celiac Disease 7
 Susceptibility to celiac disease 7 is a term allocated to a genetic defect on a particular chromosome (chromosome 1q133) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly ...read more »
71. Susceptibility to Celiac Disease 8
 Susceptibility to celiac disease 8 is a term allocated to a genetic defect on a particular chromosome (chromosome 2q11-q12) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anoma...read more »
72. Susceptibility to Celiac Disease 9
 Susceptibility to celiac disease 9 is a term allocated to a genetic defect on a particular chromosome (chromosome 3p21) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly d...read more »
73. Tetracycline - Teratogenic Agent
 There is evidence to indicate that exposure to Tetracycline during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposu...read more »
74. Tooth abscess
 Pus-filled abscess of a tooth...read more »
75. Tricho-dento-osseous syndrome
 A rare genetic disorder characterized by kinky hair, tooth enamel and bone abnormalities. There are two different subtypes with type I being distinguished from type II by the presence of a small head and increased density in the long bones....read more »
76. Tricho-dento-osseous syndrome type I
 A rare genetic ectodermal disorder characterized by kinky hair, tooth enamel and bone abnormalities....read more »
77. Turner syndrome associated Celiac Disease
 Females with Turner syndrome are more susceptible to developing celiac disease than the average population. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies am...read more »
78. Type 1 diabetes related Celiac Disease
 Patients with Type 1 diabetes are more susceptible to developing celiac disease than the average population. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies a...read more »
79. William's syndrome associated Celiac Disease
 Patients with William's syndrome are more susceptible to developing celiac disease than the average population. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varie...read more »
80. Wolcott-Rallison syndrome
 A very rare genetic condition characterized primarily by the onset of diabetes mellitus during infancy and epiphyseal dysplasia (abnormal joint development)....read more »

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