Disease Index
9,486 diseasesthoracolaryngopelvic dysplasia
Thoracolaryngopelvic dysplasia is a short-rib dysplasia characterized by thoracic dystrophy, laryngeal stenosis and a small pelvis
MeSH: C536517
Thoracolumbosacral spina bifida aperta
human disease
Thoracolumbosacral spina bifida cystica
human disease
Thoracomelic dysplasia
human disease
thromboangiitis obliterans
Human disease
MeSH: D013919
thrombocytopenia
blood platelet disease characterized by a low platelet count
MeSH: D013921
thrombocytopenia with congenital dyserythropoietic anemia
MeSH: C564525
thrombocytopenia-robin sequence syndrome
human disease
MeSH: C536898
thrombophilia due to protein S deficiency, autosomal dominant
human disease
MeSH: C567077
thrombotic microangiopathy
pathology that results in thrombosis in capillaries and arterioles, due to an endothelial injury
ICD: M31.1MeSH: D057049
thrombotic thrombocytopenic purpura
human disease
MeSH: D011697
thumb deformity-alopecia-pigmentation anomaly syndrome
human disease
MeSH: C536904
Thumb hypoplasia
congenital abnormality
thumb stiffness-brachydactyly-intellectual disability syndrome
medical condition
MeSH: C537511
thymic carcinoma
thymus cancer that derives from epithelial cells. The tumor cells in a thymic carcinoma look very different from the normal cells of the thymus, grow more quickly, and have usually spread to other parts of the body when the cancer is found
ICD: C37
thymic neuroendocrine carcinoma
Thymic neuroendocrine carcinoma is a type of thymic epithelial neoplasm (see this term) displaying evidence of neuroendocrine differentiation
thymic neuroendocrine tumor
thymic-renal-anal-lung dysplasia
This syndrome is characterised by intrauterine growth retardation, renal dysgenesis and a unilobed or absent thymus
MeSH: C536907
thymoma
thymus cancer that derives from epithelial cells
ICD: C37MeSH: D013945
Thymoma with immunodeficiency
medical condition
ICD: D84.8
thymus epithelial tumor
Human disease
MeSH: C536905
thymus neoplasm
neoplasm that affects the thymus, including thymoma and carcinoma
MeSH: D013953
thyrocerebrorenal syndrome
Thyrocerebrorenal syndrome is characterized by renal, neurologic, thyroid disease, associated with thrombocytopenia. It has been described in a brother and his sister. Intelligence was normal. It is transmitted as an autosomal recessive trait.
MeSH: C536908
thyroid cancer
endocrine gland cancer located in the thryoid gland located in the neck below the thyroid cartilage
thyroid carcinoma
thyroid cancer that has material basis in epithelial cells
Thyroid dyshormonogenesis
Familial thyroid dyshormonogenesis is a type of primary congenital hypothyroidism (see this term), a permanent thyroid hormone deficiency that is present from birth, which results from inborn errors of thyroid hormone synthesis
ICD: E07.1MeSH: C564766
thyroid ectopy
Thyroid ectopia is a form of thyroid dysgenesis (see this term) characterized by an ectopic location of the thyroid gland that results in primary congenital hypothyroidism (see this term), a permanent thyroid deficiency that is present from birth
thyroid hypoplasia
thyroid lymphoma
lymphoma primarily involving the thyroid gland
ICD: C73
thyroid medullary carcinoma
malignant thyroid neoplasm originating from C-cells
ICD: C73MeSH: C536914