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Arrhythmogenic right ventricular dysplasia 2. Arrhythmogenic right ventricular dysplasia 9. Autosomal recessive hereditary neuropathy (Charcot-Marie-Tooth disease, type 4B1). Autosomal recessive infantile malignant osteopetrosis (OPTB1). Autosomal recessive infantile malignant osteopetrosis (OPTB4). Carbonic Anhydrase Deficiency II. Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy. Chronic infantile neurological cutaneous articular (CINCA) syndrome. Crigler Najjar Syndrome, type I.

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Arrhythmogenic right ventricular dysplasia 2. Arrhythmogenic right ventricular dysplasia 9. Autosomal recessive hereditary neuropathy (Charcot-Marie-Tooth disease, type 4B1). Autosomal recessive infantile malignant osteopetrosis (OPTB1). Autosomal recessive infantile malignant osteopetrosis (OPTB4). Carbonic Anhydrase Deficiency II. Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy. Chronic infantile neurological cutaneous articular (CINCA) syndrome. Crigler Najjar Syndrome, type I.

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1 statistics

2 submission

3 feedback

4 select disease

5 achondroplasia

6 allgrove syndrome

7 androgen insensitivity syndrome

8 aniridia

9 ataxia syndrome fxtas

10 becker muscular dystrophy

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statistics,submission,feedback,select disease,achondroplasia,allgrove syndrome,androgen insensitivity syndrome,aniridia,ataxia syndrome fxtas,becker muscular dystrophy,beta thalassemia,biotidinase deficiency,cerebrotendinous xanthomatosis ctx,h syndrome

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Arrhythmogenic right ventricular dysplasia 2. Arrhythmogenic right ventricular dysplasia 9. Autosomal recessive hereditary neuropathy (Charcot-Marie-Tooth disease, type 4B1). Autosomal recessive infantile malignant osteopetrosis (OPTB1). Autosomal recessive infantile malignant osteopetrosis (OPTB4). Carbonic Anhydrase Deficiency II. Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy. Chronic infantile neurological cutaneous articular (CINCA) syndrome. Crigler Najjar Syndrome, type I.

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Arrhythmogenic right ventricular dysplasia 2. Arrhythmogenic right ventricular dysplasia 9. Autosomal recessive hereditary neuropathy (Charcot-Marie-Tooth disease, type 4B1). Autosomal recessive infantile malignant osteopetrosis (OPTB1). Autosomal recessive infantile malignant osteopetrosis (OPTB4). Carbonic Anhydrase Deficiency II. Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy. Chronic infantile neurological cutaneous articular (CINCA) syndrome. Crigler Najjar Syndrome, type I.

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