MEDLIB
Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Primary cutaneous T-cell lymphoma

ORPHA:171901Сан.

Primary cutaneous amyloidosis

ORPHA:137807Клин. топ
Autosomal dominant, Not applicable

Primary cutaneous anaplastic large cell lymphoma

ORPHA:300865Ауру

Primary cutaneous lymphoma

ORPHA:542Сан.

Primary cutaneous peripheral T-cell lymphoma not otherwise specified

ORPHA:86885Ауру
Not applicable

Primary cutaneous plasmacytosis

ORPHA:451602Ауру
Not applicable

Primary cutis verticis gyrata

ORPHA:671Клин. топ

Primary dystonia, DYT13 type

ORPHA:98807Ауру
Autosomal dominant

Primary dystonia, DYT17 type

ORPHA:370103Ауру
Autosomal recessive

Primary dystonia, DYT2 type

ORPHA:99657Ауру
Autosomal recessive

Primary dystonia, DYT21 type

ORPHA:306734Ауру
Autosomal dominant

Primary dystonia, DYT27 type

ORPHA:464440Ауру
Autosomal recessive

Primary dystonia, DYT4 type

ORPHA:98805Ауру
Autosomal dominant

Primary dystonia, DYT6 type

ORPHA:98806Ауру
Autosomal dominant

Primary effusion lymphoma

ORPHA:48686Ауру

Primary erythromelalgia

ORPHA:90026Ауру
Autosomal dominant

Primary essential cutis verticis gyrata

ORPHA:357220Ауру

Primary failure of tooth eruption

ORPHA:412206Ауру
Autosomal dominant

Primary familial polycythemia

ORPHA:90042Ауру
Autosomal dominant

Primary hepatic neuroendocrine carcinoma

ORPHA:100085Ауру
Not applicable

Primary hyperaldosteronism-seizures-neurological abnormalities syndrome

ORPHA:369929Ауру
Not applicable

Primary hypereosinophilic syndrome

ORPHA:314950Ауру

Primary hypergonadotropic hypogonadism-partial alopecia syndrome

ORPHA:2232Ауру
Autosomal recessive

Primary hyperoxaluria

ORPHA:416Ауру
Autosomal recessive