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X-linked dystonia-parkinsonism

1 OMIM reference -
1 associated gene
65 connected diseases
No signs/symptoms info

Disease	Type of connection
B-cell chronic lymphocytic leukemia
Extraskeletal myxoid chondrosarcoma
Spinocerebellar ataxia type 17
Familial retinoblastoma
Mantle cell lymphoma
Monosomy 13q14
Multiple myeloma
Unilateral retinoblastoma
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Berardinelli-Seip congenital lipodystrophy
Anaplastic ependymoma
Adrenocortical carcinoma
Essential thrombocythemia
Familial pancreatic carcinoma
Giant cell glioblastoma
Gliosarcoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Precursor B-cell acute lymphoblastic leukemia
Aniridia - cerebellar ataxia - intellectual deficit
Autosomal dominant keratitis
Foveal hypoplasia - presenile cataract
Isolated aniridia
Isolated optic nerve hypoplasia
Morning glory syndrome
Peters anomaly
WAGR syndrome
Alveolar rhabdomyosarcoma
Craniofacial-deafness-hand syndrome
Waardenburg syndrome type 1
Waardenburg syndrome type 3
Complete androgen insensitivity syndrome
Desmoplastic small round cell tumor
Ewing sarcoma
Extraskeletal Ewing sarcoma
Familial hypospadias
Kennedy disease
Melanoma of soft part
Partial androgen insensitivity syndrome
APC-related attenuated familial adenomatous polyposis
Acute necrotizing encephalopathy of childhood
Amyotrophic lateral sclerosis
Autosomal recessive limb-girdle muscular dystrophy type 2B
Autosomal recessive limb-girdle muscular dystrophy type 2D
Congenital myopathy, Paradas type
Desmoid tumor
Distal myopathy with anterior tibial onset
Familial acute necrotizing encephalopathy
Familial adenomatous polyposis due to 5q22.2 microdeletion
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Gardner syndrome
Gray platelet syndrome
Hereditary pheochromocytoma-paraganglioma
Inflammatory myofibroblastic tumor
Intellectual deficit - sparse hair - brachydactyly
Intellectual deficit, X-linked, Siderius type
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome
Miyoshi myopathy
Multiple endocrine neoplasia type 1
Turcot syndrome with polyposis
Zollinger-Ellison syndrome
Hypodontia - dysplasia of nails
Oligodontia

Synonym(s): - DYT3 - Lubag - Lubag syndrome - XDP

Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (ICD10): - Diseases of the nervous system -

Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: adult Type of inheritance: x-linked recessive		External references: 1 OMIM reference - No MeSH references

Gene symbol	UniProt reference	OMIM reference
TAF1	P21675	313650

No signs/symptoms info available.