CAUDAL REGRESSION SEQUENCE |
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CD8 DEFICIENCY, FAMILIAL |
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CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1 |
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CENANI-LENZ SYNDACTYLY SYNDROME; CLSS |
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CENTRAL CORE DISEASE OF MUSCLE; CCD |
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CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS |
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CENTRIPETALIS RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA |
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CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS |
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CEREBELLAR ATAXIA, CAYMAN TYPE; ATCAY |
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CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN |
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CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1 |
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CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 2; CAMRQ2 |
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CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 4; CAMRQ4 |
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CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR |
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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 CREATINE DEFICIENCY SYNDROME 1; CCDS1 |
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