Treft Sanborn Carey syndrome
Treft-Sanborn-Carey syndrome: A rare syndrome characterized by a variety of eye problems and deafness.
Diseases
Tremor hereditary essential- 1
Tremor hereditary essential, 1: An inherited movement disorder involving tremors which occurs mainly in the arms but other parts of the body are often involved. Any kind of stress on the body such as hunger and tiredness can aggravate the condition.
Tremor hereditary essential- 2
Tremor hereditary essential, 2: An inherited movement disorder involving tremors. Any kind of stress on the body such as hunger and tiredness can aggravate the condition.
Tremors- nystagmus and duodenal ulcers
Treponema infection
Treponema infection: A rare infectious diseases which is transmitted through sexual contact and caused by Treponema pallidum (a spirochete bacterium). Untreated cases can result in severe complications and even death.
Trichinellosis
Trichinosis, also called trichinellosis, or trichiniasis, is a parasitic disease caused by eating raw or undercooked pork and wild game infected with the larvae of a species of roundworm Trichinella spiralis, commonly called the trichina worm. The few cases in the United States are mostly the result of eating undercooked game, bear meat, or home reared pigs. It is most common in the developing world and where pigs are commonly fed raw garbage
Tricho odonto onycho dermal syndrome
Tricho odonto onycho dermal syndrome: A very rare syndrome characterized by hair, tooth, nail and skin abnormalities.
Tricho odonto onychodysplasia syndactyly dominant type
Tricho odonto onycho dermal syndrome: A very rare syndrome characterized by hair, tooth, nail and skin abnormalities.
Tricho onychic dysplasia
Tricho-onychic dysplasia: A rare genetic syndrome characterized by hair and nail abnormalities.
Tricho onycho hypohidrotic dysplasia
Tricho retino dento digital syndrome
Tricho-retino-dento-digital syndrome: A very rare syndrome characterized by hair, eye, tooth and finger abnormalities.
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
Tricho-dento-osseous syndrome 1
A rare genetic ectodermal disorder characterized by kinky hair, tooth enamel and bone abnormalities.
Tricho-hepato-enteric syndrome
Tricho-hepato-enteric syndrome (THE), also known as syndromic or phenotypic diarrhea, is an extremely rare congenital bowel disorder which manifests itself as intractable diarrhea in infants with intrauterine growth retardation, hair and facial abnormalities
Trichodental syndrome
A very rare syndrome characterized by short fine hair and dental abnormalities.
Trichodermodysplasia dental alterations
A rare syndrome characterized mainly by hair, skin and tooth abnormalities.
Trichodysplasia xeroderma
A rare disorder involving the skin and hair .
Trichoepithelioma multiple familial
An inherited skin disorder characterized by a number of small tumors that occur on the face. The number of tumors is variable with most of the face being covered in some cases.
Trichofolliculoma
A benign hair tumor which looks like a small lump with a tuft of hair growing out of it. The hair is often white and short. They often occur around the nose area.
Trichomalacia
A rare genetic condition resulting in patchy hair loss in children. It is an abnormality of the hair shaft and can be due to a compulsive habit of pulling hair on the head or even eyelashes and eyebrows
Trichomegaly cataract hereditary spherocytosis
A rare syndrome characterized mainly by cataracts, excessive eyelash growth and and a blood abnormality (the red blood cells are spherical instead of doughnut shaped which makes them fragile).
Trichomegaly with mental retardation- dwarfism and pigmentary degeneration of retina
A rare genetic condition characterized by mental retardation, dwarfism, retinal pigmentary degeneration and hairy eyelashes and eyebrows.
Trichoodontoonychial dysplasia
Trichorhinophalangeal syndrome type 1
A rare genetic disorder characterized by bulbous nose, sparse hair and coning of epiphyses
Trichorhinophalangeal syndrome type 2
A rare genetic disorder characterized by bony growths, bulbous nose, distinctive facial features and loose excess skin during infancy.
Trichorhinophalangeal syndrome type 3
A rare inherited disorder involving hair, face, teeth, and bone abnormalities.
Trichorrhexis nodosa syndrome
Trichorrhexis nodosa is a problem in which thickened or weak points (nodes) along the hair shaft cause your hair to break off easily.
Trichoscyphodysplasia
A rare inherited skeletal disorder involving abnormal bone development which results in short stature, short hands and feet and alopecia is also present.
Trichostasis spinulosa
Trichostasis spinulosa is also called “bundle bush hair”. Instead of one hair protruding from a hair follicle, bundle or bush of hair come out of a single follicle. It has no pathological significance.
Trichothiodystrophy
A rare inherited skin disorder characterized by red, dry, scaly skin (I - ichthyosis), brittle hair (B), impaired physical and mental development (I), decreased fertility (D) and short stature (S). It is the same as PIBIDS syndrome but doesn't involve photosensitivity.