hereditary cerebellar ataxia
81atrophy — atrophic /euh trof ik, euh troh fik/, adj. /a treuh fee/, n., v., atrophied, atrophying. n. 1. Also, atrophia /euh troh fee euh/. Pathol. a wasting away of the body or of an organ or part, as from defective nutrition or nerve damage. 2.… …
82Refsum disease — Classification and external resources Phytanic acid ICD 10 G60.1 …
83Creutzfeldt–Jakob disease — Classification and external resources Tonsil biopsy in variant CJD. Prion Protein immunostaining. ICD 10 A …
84Neurofibromatosis type I — For Von Recklinghausen s disease of bone, a disorder seen with hyperparathyroidism, see osteitis fibrosa cystica. Neurofibromatosis type 1 Classification and external resources ICD 10 Q85.0 (ILDS Q85.010) ICD …
85Chromosome 9 (human) — Chromosome 9 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome, as they normally do with all chromosomes. Chromosome 9 spans about 145 million base pairs of nucleic acids (the building blocks of… …
86Refsum's disease — Infobox Disease Name = PAGENAME Caption = Phytanic acid DiseasesDB = 11213 ICD10 = ICD10|G|60|1|g|60 ICD9 = ICD9|356.3 ICDO = OMIM = 266500 MedlinePlus = eMedicineSubj = derm eMedicineTopic = 705 MeshID = D012035 Refsum s disease (Refsum Thiébaut …
87Erdheim–Chester disease — Erdheim Chester disease Classification and external resources ICD 10 C96.1 ICD …
88MELAS syndrome — Mitochondrial myopathy, encephalomyopathy, lactic acidosis, and stroke like episodes Classification and external resources Basal ganglia calcification, cerebellar atrophy, increased …
