| T cell immunodeficiency primary |
| TRAPS (TNF-receptor-associated periodic syndrome) |
| Taurodontia absent teeth sparse hair |
| Teebi Naguib Alawadi syndrome |
| Teeth noneruption of with maxillary hypoplasia and genu valgum |
| Tel Hashomer camptodactyly syndrome |
| Telangiectasia ataxia variant V1 |
| Telangiectasia, hereditary hemorrhagic |
| Telecanthus hypertelorism pes cavus |
| Telecanthus with associated abnormalities |
| Telencephalic leukoencephalopathy |
| Telfer Sugar Jaeger syndrome |
| Temporal epilepsy, familial |
| Temporomandibular ankylosis |
| Temporomandibular joint dysfunction (TMJ) |
| Ter Haar Hamel Hendricks syndrome |
| Tethered spinal cord disease |
| Tetraamelia ectodermal dysplasia |
| Tetraamelia multiple malformations |
| Tetraamelia pulmonary hypoplasia |
| Tetrahydrobiopterin deficiencies |
| Thalamic degeneration symmetrical infantile |
| Thalamic degenerescence infantile |
| Thanatophoric dysplasia Glasgow variant |
| Thanatophoric dysplasia cloverleaf skull |
| Thanos Stewart Zonana syndrome |
| Theodor Hertz Goodman syndrome |
| Thiemann epiphyseal disease |
| Thin ribs tubular bones dysmorphism |
| Thiopurine S methyltranferase deficiency |
| Thomas Jewett Raines syndrome |
| Thompson Baraitser syndrome |
| Thong Douglas Ferrante syndrome |
| Thoracic dysplasia hydrocephalus syndrome |
| Thoraco abdominal enteric duplication |
| Thoraco limb dysplasia Rivera type |
| Thoracolaryngopelvic dysplasia |
| Thost-Unna palmoplantar keratoderma |
| Thrombocytopathy asplenia miosis |
| Thrombocytopenia Robin sequence |
| Thrombocytopenia cerebellar hypoplasia short stature |
| Thrombocytopenia chromosome breakage |
| Thrombocytopenia multiple congenital anomaly |
| Thrombocytopenic purpura, autoimmune |
| Thrombomodulin anomalies, familial |
| Thrombotic microangiopathy, familial |
| Thumb absence hypoplastic halluces |
| Thumb absent short stature immune deficiency |
| Thumb deformity, alopecia, pigmentation anomaly |
| Thumb stiff brachydactyly mental retardation |
| Thymic renal anal lung dysplasia |
| Thyrocerebrorenal syndrome |
| Thyroid carcinoma, follicular |
| Thyroid carcinoma, papillary (TPC) |
| Thyroid hormone plasma membrane transport defect |
| Thyroid, renal and digital anomalies |
| Tibia absent polydactyly arachnoid cyst |
| Tibiae bowed radial anomalies osteopenia fracture |
| Tibial aplasia ectrodactyly |
| Tibial aplasia ectrodactyly hydrocephalus |
| Tibial hemimelia cleft lip palate |
| Tollner Horst Manzke syndrome |
| Toluene antenatal infection |
| Tome Brune Fardeau syndrome |
| Toni Debre Fanconi maladie |
| Toriello Lacassie Droste syndrome |
| Toriello-Higgins-Miller syndrome |
| Torticollis keloids cryptorchidism renal dysplasia |
| Tosti Misciali Barbareschi syndrome |
| Total Hypotrichosis, Mari type |
| Touraine-Solente-Gole syndrome |
| Toxopachyoteose diaphysaire tibio peroniere |
| Tracheobronchopathia osteoplastica |
| Tracheoesophageal fistula |
| Tracheoesophageal fistula symphalangism |
| Tracheophageal fistula hypospadias |
| Tranebjaerg Svejgaard syndrome |
| Transcobalamin II deficiency |
| Transient erythroblastopenia of childhood |
| Transient neonatal arthrogryposis |
| Transitional cell carcinoma |
| Transplacental infections |
| Transposition of great vessels |
| Transverse limb deficiency hemangioma |
| Treacher Collins syndrome |
| Treft Sanborn Carey syndrome |
| Tremor hereditary essential |
| Tricho dento osseous syndrome type 1 |
| Tricho odonto onycho dermal syndrome |
| Tricho odonto onychodysplasia syndactyly dominant type |
| Tricho onycho hypohidrotic dysplasia |
| Tricho retino dento digital syndrome |
| Tricho-dento-osseous syndrome |
| Tricho-hepato-enteric syndrome |
| Trichodermodysplasia dental alterations |
| Trichodysplasia xeroderma |
| Trichoepithelioma multiple familial |
| Trichomegaly cataract hereditary spherocytosis |
| Trichomegaly retina pigmentary degeneration dwarfi |
| Trichoodontoonychial dysplasia |
| Trichorhinophalangeal syndrome type I |
| Trichorhinophalangeal syndrome type II |
| Trichorhinophalangeal syndrome type III |
| Trichothiodystrophy sun sensitivity |
| Trigonocephaly bifid nose acral anomalies |
| Trigonocephaly broad thumbs |
| Trigonocephaly ptosis coloboma |
| Trigonocephaly ptosis mental retardation |
| Trigonomacrocephaly tibial defect polydactyly |
| Trihydroxycholestanoylcoa oxidase isolated deficiency |
| Trimethadione antenatal infection |
| Triose phosphate-isomerase deficiency |
| Triphalangeal thumb non opposable |
| Triphalangeal thumb polysyndactyly syndrome |
| Triphalangeal thumbs brachyectrodactyly |
| Trismus pseudocamptodactyly syndrome |
| Trophoblastic Neoplasms (gestational trophoblastic disease) |
| Tropical Spastic Paraparesis |
| Trueb Burg Bottani syndrome |
| Trypanosomiasis, east-African |
| Trypanosomiasis, west African |
| Tsukahara Azuno Kajii syndrome |
| Tuberous Sclerosis, type 1 |
| Tuberous Sclerosis, type 2 |
| Tunglang Savage Bellman syndrome |
| Twin twin transfusion syndrome |
| Tyrosine-oxidase temporary deficiency |
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