188011
|
|
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T-complex 11 family, X-linked 1 |
- |
Curated: N/A
Unreviewed: N/A
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188012
|
|
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T-complex 11 family, X-linked 2 |
- |
Curated: N/A
Unreviewed: N/A
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188013
|
|
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T-complex 11 family, X-linked 3, pseudogene |
- |
Curated: N/A
Unreviewed: N/A
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188014
|
|
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T-complex 1 pseudogene 1 |
CCT1-3P, TCP1L1 |
Curated: N/A
Unreviewed: N/A
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188015
|
|
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T-complex 1 pseudogene 2 |
CCT1-2P, TCP1L2 |
Curated: N/A
Unreviewed: N/A
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188016
|
|
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T-complex 1 pseudogene 3 |
CCT1-1P, TCP1L3 |
Curated: N/A
Unreviewed: N/A
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188017
|
|
|
- |
- |
Curated: N/A
Unreviewed: Hypothyroidism, Thyroid dyshormonogenesis
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188018
|
|
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T cell leukemia translocation altered |
- |
Curated: N/A
Unreviewed: Crohn Disease, Hematologic neoplasm, Hyperuricemia, Myeloid leukemia, Pancreatic neoplasm, Schizophrenia, T-cell leukemia
|
188019
|
|
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Tectonic family member 1 |
JBTS13, TECT1 |
Curated: Atrial fibrillation, Developmental disability, Aplasia of the vermis, Global developmental delay, Joubert syndrome, Meckel-gruber syndrome
Unreviewed: Cerebellar vermis agenesis, Ciliopathies, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Congenital Cerebral Hernia, Congenital Coloboma Of Iris, Developmental Delay, Disorder Of Eye, Esophageal squamous cell carcinoma, Esophagus Neoplasm, Glioblastoma, Glioma, Hirschsprung Disease, Holoprosencephaly, Hydrocephalus, Joubert Syndrome, Lung carcinoma, Meckel Syndrome, Meckel-Gruber Syndrome, Mental retardation, Neoplasms, Nystagmus, Occipital Encephalocele, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Oral cleft, Orofaciodigital syndrome, Pachygyria, Pancreatic cancer, Pancreatic carcinoma, Polydactyly Of Toes, Polymicrogyria, Prostate cancer, Prostatic neoplasm, Ptosis, Scoliosis, Situs Inversus, Squamous cell carcinoma, Stomach Carcinoma, Stomach Neoplasms, Strabismus, Thyroid cancer, Thyroid Carcinoma, Thyroid Neoplasm
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188020
|
|
|
Tectonic family member 2 |
C12orf38, JBTS24, MKS8, TECT2 |
Curated: Cystic kidney disease, Desbuquois syndrome, Aplasia of the vermis, Joubert syndrome, Meckel-gruber syndrome, Joubert syndrome 24
Unreviewed: Anencephaly, Asplenia, Cataract, Cerebellar Hypoplasia, Cerebellar vermis agenesis, Ciliopathies, Ciliopathy, Congenital Cerebral Hernia, Congenital Clubfoot, Congenital Coloboma Of Iris, Congenital Hepatic Fibrosis, Cryptorchidism, Cystic liver disease, Dandy-Walker Syndrome, Developmental Delay, Disorder Of Eye, Double Ureter, Fibrosis Of Pancreas, Foot Polydactyly, Hirschsprung Disease, Hydrocephalus, Hyperopia, Joubert Syndrome, Lobar Holoprosencephaly, Male Pseudohermaphroditism, Meckel Syndrome, Meckel-Gruber Syndrome, Mental retardation, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Multicystic renal dysplasia, Neoplasms, Nephronophthisis, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Optic Atrophy, Oral cleft, Ovarian cancer, Pachygyria, Pancreatic Cyst, Polycystic liver disease, Polydactyly, Polydactyly Of Toes, Polymicrogyria, Postaxial hand polydactyly, Ptosis, Sclerocornea, Scoliosis, Situs Inversus, Strabismus, Syndromic microphthalmia, Talipes, True Hermaphroditism, Urethral atresia
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