AL amyloidosis
|
(Orphanet:85443)
|
AORTIC ANEURYSM, FAMILIAL THORACIC 4
|
(OMIM:132900)
|
Alkaptonuria
|
(Orphanet:56)
|
Arterial tortuosity syndrome
|
(Orphanet:3342)
|
Babesiosis
|
(Orphanet:108)
|
Bannayan-Riley-Ruvalcaba syndrome
|
(Orphanet:109)
|
Bardet-Biedl syndrome 2
|
(OMIM:615981)
|
Behçet disease
|
(Orphanet:117)
|
Berardinelli-Seip congenital lipodystrophy
|
(Orphanet:528)
|
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
|
(OMIM:608320)
|
Cardiomyopathy, dilated, 1S
|
(OMIM:613426)
|
Cerebrotendinous xanthomatosis
|
(Orphanet:909)
|
Chronic hiccup
|
(Orphanet:396)
|
Cogan syndrome
|
(Orphanet:1467)
|
Combined pulmonary fibrosis-emphysema syndrome
|
(Orphanet:300564)
|
Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis
|
(Orphanet:94062)
|
Cutaneous mastocytosis
|
(Orphanet:66646)
|
Dermatomyositis
|
(Orphanet:221)
|
Eosinophilic granulomatosis with polyangiitis
|
(Orphanet:183)
|
Essential thrombocythemia
|
(Orphanet:3318)
|
Fabry disease
|
(Orphanet:324)
|
Familial Mediterranean fever
|
(Orphanet:342)
|
Familial cutaneous collagenoma
|
(Orphanet:53296)
|
Familial partial lipodystrophy associated with PPARG mutations
|
(Orphanet:79083)
|
Familial partial lipodystrophy due to AKT2 mutations
|
(Orphanet:79085)
|
Familial partial lipodystrophy, Dunnigan type
|
(Orphanet:2348)
|
Familial partial lipodystrophy, Köbberling type
|
(Orphanet:79084)
|
Fish-eye disease
|
(Orphanet:79292)
|
Gastrocutaneous syndrome
|
(Orphanet:2069)
|
Giant cell arteritis
|
(Orphanet:397)
|
Granulomatosis with polyangiitis
|
(Orphanet:900)
|
HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, TYPE B
|
(OMIM:144010)
|
Hurler syndrome
|
(Orphanet:93473)
|
Hutchinson-Gilford progeria syndrome
|
(Orphanet:740)
|
Hypoalphalipoproteinemia
|
(Orphanet:31153)
|
Juvenile dermatomyositis
|
(Orphanet:93672)
|
Kawasaki disease
|
(Orphanet:2331)
|
Lyell syndrome
|
(Orphanet:537)
|
Malignant atrophic papulosis
|
(Orphanet:679)
|
Maturity-onset diabetes of the young, type 3
|
(OMIM:600496)
|
Noonan syndrome with multiple lentigines
|
(Orphanet:500)
|
Polyarteritis nodosa
|
(Orphanet:767)
|
Polycythemia vera
|
(Orphanet:729)
|
Polymyositis
|
(Orphanet:732)
|
Primary familial polycythemia
|
(Orphanet:90042)
|
Primary lipodystrophy
|
(Orphanet:90970)
|
Primary systemic amyloidosis
|
(Orphanet:314701)
|
Pseudoxanthoma elasticum
|
(Orphanet:758)
|
Relapsing polychondritis
|
(Orphanet:728)
|
Scleroderma
|
(Orphanet:801)
|
Senile systemic amyloidosis
|
(Orphanet:330001)
|
Stevens-Johnson syndrome
|
(Orphanet:36426)
|
TRAPS syndrome
|
(Orphanet:32960)
|
Takayasu arteritis
|
(Orphanet:3287)
|
Tako-Tsubo cardiomyopathy
|
(Orphanet:66529)
|
Werner syndrome
|
(Orphanet:902)
|
Williams syndrome
|
(Orphanet:904)
|
[DEL] PSEUDOXANTHOMA ELASTICUM
|
(OMIM:264800)
|