MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Primary cutaneous T-cell lymphoma

ORPHA:171901Kat.

Primary cutaneous amyloidosis

ORPHA:137807Kl. gruppe
Autosomal dominant, Not applicable

Primary cutaneous anaplastic large cell lymphoma

ORPHA:300865Kr.

Primary cutaneous lymphoma

ORPHA:542Kat.

Primary cutaneous peripheral T-cell lymphoma not otherwise specified

ORPHA:86885Kr.
Not applicable

Primary cutaneous plasmacytosis

ORPHA:451602Kr.
Not applicable

Primary cutis verticis gyrata

ORPHA:671Kl. gruppe

Primary dystonia, DYT13 type

ORPHA:98807Kr.
Autosomal dominant

Primary dystonia, DYT17 type

ORPHA:370103Kr.
Autosomal recessive

Primary dystonia, DYT2 type

ORPHA:99657Kr.
Autosomal recessive

Primary dystonia, DYT21 type

ORPHA:306734Kr.
Autosomal dominant

Primary dystonia, DYT27 type

ORPHA:464440Kr.
Autosomal recessive

Primary dystonia, DYT4 type

ORPHA:98805Kr.
Autosomal dominant

Primary dystonia, DYT6 type

ORPHA:98806Kr.
Autosomal dominant

Primary effusion lymphoma

ORPHA:48686Kr.

Primary erythromelalgia

ORPHA:90026Kr.
Autosomal dominant

Primary essential cutis verticis gyrata

ORPHA:357220Kr.

Primary failure of tooth eruption

ORPHA:412206Kr.
Autosomal dominant

Primary familial polycythemia

ORPHA:90042Kr.
Autosomal dominant

Primary hepatic neuroendocrine carcinoma

ORPHA:100085Kr.
Not applicable

Primary hyperaldosteronism-seizures-neurological abnormalities syndrome

ORPHA:369929Kr.
Not applicable

Primary hypereosinophilic syndrome

ORPHA:314950Kr.

Primary hypergonadotropic hypogonadism-partial alopecia syndrome

ORPHA:2232Kr.
Autosomal recessive

Primary hyperoxaluria

ORPHA:416Kr.
Autosomal recessive