Lista chorób rzadkich*

97678 - Maternal uniparental disomy of chromosome 13

97685 - 17q11 microdeletion syndrome

97927 - OBSOLETE: Peripheral resistance to thyroid hormones

97929 - Rare cardiac disease

97935 - Rare gastroenterologic disease

97944 - Gastroduodenal malformation

97945 - Intestinal malformation

97955 - Rare respiratory disease

97957 - Respiratory or thoracic malformation

97962 - Rare surgical thoracic disease

97965 - Rare surgical cardiac disease

97966 - Rare ophthalmic disorder

97978 - Rare endocrine disease

97992 - Rare hematologic disease

98004 - Rare immune disease

98006 - Rare neurologic disease

98010 - Infectious disease of the nervous system

98022 - Rare headache

98023 - Rare systemic or rheumatologic disease

98026 - Rare odontologic disease

98027 - Rare disease with odontological manifestation

98028 - Rare circulatory system disease

98033 - Rare neurologic disease with psychiatric involvement

98036 - Rare otorhinolaryngologic disease

98038 - Cranial malformation

98039 - Digestive tract malformation

98041 - Visceral malformation of the liver, biliary tract, pancreas or spleen

98043 - Diaphragmatic or abdominal wall malformation

98044 - Central nervous system malformation

98045 - Respiratory or mediastinal malformation

98047 - Rare infertility

98048 - Rare male infertility

98049 - Rare female infertility

98050 - Rare allergic disease

98052 - Rare allergic respiratory disease

98053 - Rare genetic disease

98054 - Rare genetic cardiac disease

98056 - Rare genetic renal disease

98057 - Rare tumor

98058 - Rare urinary tract tumor

98059 - Rare digestive tumor

98060 - Rare respiratory tumor

98061 - Rare otorhinolaryngologic tumor

98062 - Rare nervous system tumor

98063 - Rare gynecological tumor

98064 - OBSOLETE: Rare disease in physical medicine and rehabilitation

98068 - OBSOLETE: Autosomal dominant spinocerebellar ataxia due to a polyglutamine anomaly

98069 - OBSOLETE: Autosomal dominant spinocerebellar ataxia due to a channelopathy

98070 - OBSOLETE: Autosomal dominant spinocerebellar ataxia due to repeat expansions that do not encode polyglutamine

98071 - OBSOLETE: Autosomal dominant spinocerebellar ataxia due to a point mutation

Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl

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