MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Primary cutaneous T-cell lymphoma

ORPHA:171901Cat.

Primary cutaneous amyloidosis

ORPHA:137807Clin. grp.
Autosomal dominant, Not applicable

Primary cutaneous anaplastic large cell lymphoma

ORPHA:300865Disease

Primary cutaneous lymphoma

ORPHA:542Cat.

Primary cutaneous peripheral T-cell lymphoma not otherwise specified

ORPHA:86885Disease
Not applicable

Primary cutaneous plasmacytosis

ORPHA:451602Disease
Not applicable

Primary cutis verticis gyrata

ORPHA:671Clin. grp.

Primary dystonia, DYT13 type

ORPHA:98807Disease
Autosomal dominant

Primary dystonia, DYT17 type

ORPHA:370103Disease
Autosomal recessive

Primary dystonia, DYT2 type

ORPHA:99657Disease
Autosomal recessive

Primary dystonia, DYT21 type

ORPHA:306734Disease
Autosomal dominant

Primary dystonia, DYT27 type

ORPHA:464440Disease
Autosomal recessive

Primary dystonia, DYT4 type

ORPHA:98805Disease
Autosomal dominant

Primary dystonia, DYT6 type

ORPHA:98806Disease
Autosomal dominant

Primary effusion lymphoma

ORPHA:48686Disease

Primary erythromelalgia

ORPHA:90026Disease
Autosomal dominant

Primary essential cutis verticis gyrata

ORPHA:357220Disease

Primary failure of tooth eruption

ORPHA:412206Disease
Autosomal dominant

Primary familial polycythemia

ORPHA:90042Disease
Autosomal dominant

Primary hepatic neuroendocrine carcinoma

ORPHA:100085Disease
Not applicable

Primary hyperaldosteronism-seizures-neurological abnormalities syndrome

ORPHA:369929Disease
Not applicable

Primary hypereosinophilic syndrome

ORPHA:314950Disease

Primary hypergonadotropic hypogonadism-partial alopecia syndrome

ORPHA:2232Disease
Autosomal recessive

Primary hyperoxaluria

ORPHA:416Disease
Autosomal recessive