The search resulted in 41 diseases.
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