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Orphanet:1344 | Atrial standstill | ||
Orphanet:168956 | Hypereosinophilic syndrome | ||
Orphanet:2022 | Endomyocardial fibroelastosis | ||
Orphanet:2072 | Gaucher disease - ophthalmoplegia - cardiovascular calcification | ||
Orphanet:2119 | HEC syndrome | ||
Orphanet:217635 | Familial restrictive cardiomyopathy | ||
Orphanet:217638 | Lysosomal disease with restrictive cardiomyopathy | ||
Orphanet:217720 | Non-familial restrictive cardiomyopathy | ||
Orphanet:220393 | Diffuse cutaneous systemic sclerosis | ||
Orphanet:220402 | Limited cutaneous systemic sclerosis | ||
Orphanet:220407 | Limited systemic sclerosis | ||
Orphanet:308552 | Glycogen storage disease due to acid maltase deficiency, infantile onset | ||
Orphanet:309252 | Atypical Gaucher disease due to saposin C deficiency | ||
Orphanet:314950 | Primary hypereosinophilic syndrome | ||
Orphanet:314962 | Secondary hypereosinophilic syndrome | ||
Orphanet:314970 | Lymphoid hypereosinophilic syndrome | ||
Orphanet:324 | Fabry disease | ||
Orphanet:3260 | Idiopathic hypereosinophilic syndrome | ||
Orphanet:355 | Gaucher disease | ||
Orphanet:365 | Glycogen storage disease due to acid maltase deficiency | ||
Orphanet:75249 | Familial isolated restrictive cardiomyopathy | ||
Orphanet:75565 | Tropical endomyocardial fibrosis | ||
Orphanet:75566 | Loeffler endocarditis | ||
Orphanet:758 | Pseudoxanthoma elasticum | ||
Orphanet:77259 | Gaucher disease type 1 | ||
Orphanet:77260 | Gaucher disease type 2 | ||
Orphanet:77261 | Gaucher disease type 3 | ||
Orphanet:797 | Sarcoidosis | ||
Orphanet:85212 | Fetal Gaucher disease | ||
Orphanet:85445 | AA amyloidosis |