Diseases
Name | Orphanumber | Description | XREF(s) |
---|---|---|---|
Triple A syndrome | 869 | Triple A syndrome is a very rare… | Orphanet, ICD-10, OMIM, OMIM, MeSH, MeSH |
Trismus-pseudocamptodactyly syndrome | 3377 | A rare, genetic, distal arthrogryposis… | Orphanet, OMIM, ICD-10 |
Trisomy 13 | 3378 | Trisomy 13 is a chromosomal anomaly… | Orphanet |
Trisomy 18 | 3380 | Trisomy 18 is a chromosomal abnormality… | Orphanet |
Tritanopia | 88629 | Tritanopia is an extremely rare form of… | Orphanet, ICD-10, OMIM |
Tropical pancreatitis | 103918 | A rare pancreatic disease of juvenile… | Orphanet, OMIM, ICD-10 |
Truncus arteriosus | 3384 | Truncus arteriosus (TA) is a rare… | Orphanet, OMIM, ICD-10 |
TSH-secreting pituitary adenoma | 91347 | A rare, functioning, pituitary adenoma… | Orphanet, ICD-10 |
Tuberculosis | 3389 | Tuberculosis (TB) is a contagious-… | Orphanet, ICD-10, ICD-10, MeSH, MedDRA, OMIM |
Tuberous sclerosis complex | 805 | A rare neurocutaneous disorder… | Orphanet, ICD-10, OMIM, OMIM, MeSH, MedDRA |
Tubular aggregate myopathy | 2593 | A rare congenital myopathy… | Orphanet, ICD-10, OMIM, OMIM |
Tubulinopathy-associated dysgyria | 467166 | A rare genetic central nervous system… | Orphanet |
Tufted angioma | 1063 | A rare vascular tumour that may be… | Orphanet, OMIM, MeSH, ICD-10 |
Tumor necrosis factor receptor 1 associated periodic syndrome | 32960 | Tumor necrosis factor receptor 1… | Orphanet, ICD-10, OMIM |
Turcot syndrome with polyposis | 99818 | Turcot syndrome with polyposis or… | OMIM |
Turcot syndrome with polyposis | 99818 | Turcot syndrome with polyposis or… | Orphanet, OMIM, ICD-10 |
Typical nemaline myopathy | 171436 | Typical nemaline myopathy is a moderate… | Orphanet, OMIM, OMIM, OMIM, OMIM, OMIM, OMIM, ICD-10 |
Typical urticaria pigmentosa | 158766 | Orphanet, ICD-10 | |
Tyrosinemia type 1 | 882 | Tyrosinemia type 1 (HTI) is an inborn… | Orphanet, OMIM, MedDRA, ICD-10 |
Tyrosinemia type 2 | 28378 | Tyrosinemia type 2 is an inborn error… | Orphanet, OMIM, MedDRA, ICD-10 |