| Disease Browser
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Parent Node:
 hereditary ataxia (MONDO:0000557) |
Parent Node:
inherited tremor disorder (MONDO:0017663) |
Parent Node:
X-linked disease (MONDO:0000425) |
..Starting node
.. X-linked cerebellar ataxia ()
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Child Nodes:
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| ........Arts syndrome () |
| ........ataxia - deafness - intellectual disability syndrome () |
| ........Christianson syndrome () |
| ........fragile X-associated tremor/ataxia syndrome () |
| ........spinocerebellar ataxia, X-linked 2 () |
| ........X-linked intellectual disability-ataxia-apraxia syndrome () |
| ........X-linked non progressive cerebellar ataxia () |
| ........X-linked progressive cerebellar ataxia () |
| ........X-linked sideroblastic anemia with ataxia () |
| ........X-linked spinocerebellar ataxia type 3 () |
| ........X-linked spinocerebellar ataxia type 4 () |
Sister Nodes: |
..Aarskog-Scott syndrome, X-linked ()
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..choroideremia ()
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..cone dystrophy, X-linked, with tapetal-like sheen ()
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..diabetes insipidus, nephrogenic, X-linked ()
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..dyskeratosis congenita, X-linked ()
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..epidermodysplasia verruciformis, X-linked ()
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..exudative vitreoretinopathy 2, X-linked ()
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..hemophilia A ()
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..macular dystrophy, X-linked ()
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..non-syndromic X-linked intellectual disability ()
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..Ogden syndrome ()
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..Wiskott-Aldrich syndrome ()
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..X-linked acrogigantism due to Xq26 microduplication ()
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..X-linked adrenoleukodystrophy ()
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..X-linked Alport syndrome ()
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..X-linked central congenital hypothyroidism with late-onset testicular enlargement ()
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..X-linked cerebellar ataxia ()
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..X-linked chondrodysplasia punctata ()
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..X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome ()
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..X-linked cone-rod dystrophy ()
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..X-linked congenital hemolytic anemia ()
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..X-linked congenital stationary night blindness ()
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..X-linked distal hereditary motor neuropathy ()
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..X-linked dominant disease ()
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..X-linked Ehlers-Danlos syndrome ()
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..X-linked Emery-Dreifuss muscular dystrophy ()
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..X-linked erythropoietic protoporphyria ()
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..X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome ()
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..X-linked hyper-IgM syndrome ()
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..X-linked hypohidrotic ectodermal dysplasia ()
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..X-linked hypophosphatemic rickets (recessive or dominant) ()
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..X-linked ichthyosis syndrome ()
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..X-linked lethal multiple pterygium syndrome ()
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..X-linked lymphoproliferative syndrome ()
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..X-linked nonsyndromic deafness ()
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..X-linked Opitz G/BBB syndrome ()
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..X-linked recessive disease ()
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..X-linked retinoschisis ()
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..X-linked severe congenital neutropenia ()
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..X-linked sideroblastic anemia ()
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..X-linked spondyloepimetaphyseal dysplasia ()
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..X-linked syndromic intellectual disability ()
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Further data from MedGen, OMIM,ClinVar, CTD
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