CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES; CADEDS |
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CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR |
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CEREBELLOFACIODENTAL SYNDROME; CFDS |
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CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 2 |
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CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1; CADASIL1 |
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CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL |
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CEREBRAL CAVERNOUS MALFORMATIONS 2; CCM2 |
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CEREBRAL CREATINE DEFICIENCY SYNDROME 1; CCDS1 |
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CEREBRAL CREATINE DEFICIENCY SYNDROME 2; CCDS2 |
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CEREBRAL CREATINE DEFICIENCY SYNDROME 3; CCDS3 |
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CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMA SYNDROME |
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CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 1; CPSQ1 |
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CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3; CPSQ3 |
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CEREBROCOSTOMANDIBULAR SYNDROME; CCMS |
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CEREBROOCULOFACIOSKELETAL SYNDROME 1; COFS1 |
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CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 1; CRMCC1 |
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CEREBROTENDINOUS XANTHOMATOSIS; CTX |
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CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10 |
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CEROID LIPOFUSCINOSIS, NEURONAL, 11; CLN11 |
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CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13 |
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