Disease Index
9,486 diseasestotal spina bifida cystica
human disease
Tourette syndrome
neurodevelopmental condition
ICD: F95.295.2.MeSH: D005879
Townes-Brocks syndrome
genetic disorder
ICD: Q87.8MeSH: C536974
toxic dermatosis
human disease
toxic epidermal necrolysis
Severe skin reaction
ICD: L51.2
toxic oil syndrome
foodborne illness
toxic shock syndrome
condition caused by bacterial toxins
toxin-mediated infectious botulism
leading to toxin-mediated infection. Infectious botulism includes wound botulism and intestinal toxemia botulism (infant botulism and adult intestinal botulism; see these terms).
toxocariasis
Illness of humans caused by larvae of the dog, the cat or the fox roundworm
MeSH: D014120
Tracheal agenesis
congenital disorder of respiratory system
MeSH: C536975
tracheal anomaly
human disease
ICD: Q32.1
Tracheo-esophageal fistula-hypospadias syndrome
human disease
tracheobronchomegaly
congenital disorder of respiratory system
MeSH: D014137
tracheobronchopathia osteochondroplastica
medical condition
ICD: J98.0MeSH: C536977
tracheoesophageal fistula
congenital disorder of digestive system
ICD: J95.0MeSH: D014138
tracheomalacia
tracheal disease
MeSH: D055090
transaldolase deficiency
medical condition
MeSH: C563207
transcobalamin 1 deficiency
human disease
MeSH: C562798
transcobalamin II deficiency
vitamin B12 deficiency that is characterized by a lack of vitamin B12 intestinal absorption resulting from a deficiency in the B12 transport protein TCII
transgrediens et progrediens palmoplantar keratoderma
human disease
transient bullous dermolysis of the newborn
Transient bullous dermolysis of the newborn is a rare subtype of dystrophic epidermolysis bullosa (DEB, see this term) characterized by generalized blistering at birth that usually regresses within the first 6 to 24 months of life
MeSH: C536979
transient congenital hypothyroidism
human disease
transient congenital hypothyroidism due to maternal factor
human disease
transient congenital hypothyroidism due to neonatal factor
human disease
Transient erythroblastopenia of childhood
medical condition
MeSH: C536980
transient hyperammonemia of the newborn
human disease
transient hypogammaglobulinemia of infancy
form of hypogammaglobulinemia appearing after birth, leading to a reduction in the level of IgG, and also sometimes IgA and IgM
transient infantile hypertriglyceridemia and hepatosteatosis
human disease
transient myeloproliferative syndrome
myeloproliferative neoplasm characterized by leukocytosis in newborns with Down syndrome and rarely in non-Down's infants
ICD: D47.7
transient neonatal diabetes mellitus
neonatal diabetes mellitus characterized by hyperglycemia during the neonatal period that remits during infancy but recurs in later life in most patients
MeSH: C563322