MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Primary cutaneous T-cell lymphoma

ORPHA:171901Категория

Primary cutaneous amyloidosis

ORPHA:137807Клин. группа
Autosomal dominant, Not applicable

Primary cutaneous anaplastic large cell lymphoma

ORPHA:300865Заболевание

Primary cutaneous lymphoma

ORPHA:542Категория

Primary cutaneous peripheral T-cell lymphoma not otherwise specified

ORPHA:86885Заболевание
Not applicable

Primary cutaneous plasmacytosis

ORPHA:451602Заболевание
Not applicable

Primary cutis verticis gyrata

ORPHA:671Клин. группа

Primary dystonia, DYT13 type

ORPHA:98807Заболевание
Autosomal dominant

Primary dystonia, DYT17 type

ORPHA:370103Заболевание
Autosomal recessive

Primary dystonia, DYT2 type

ORPHA:99657Заболевание
Autosomal recessive

Primary dystonia, DYT21 type

ORPHA:306734Заболевание
Autosomal dominant

Primary dystonia, DYT27 type

ORPHA:464440Заболевание
Autosomal recessive

Primary dystonia, DYT4 type

ORPHA:98805Заболевание
Autosomal dominant

Primary dystonia, DYT6 type

ORPHA:98806Заболевание
Autosomal dominant

Primary effusion lymphoma

ORPHA:48686Заболевание

Primary erythromelalgia

ORPHA:90026Заболевание
Autosomal dominant

Primary essential cutis verticis gyrata

ORPHA:357220Заболевание

Primary failure of tooth eruption

ORPHA:412206Заболевание
Autosomal dominant

Primary familial polycythemia

ORPHA:90042Заболевание
Autosomal dominant

Primary hepatic neuroendocrine carcinoma

ORPHA:100085Заболевание
Not applicable

Primary hyperaldosteronism-seizures-neurological abnormalities syndrome

ORPHA:369929Заболевание
Not applicable

Primary hypereosinophilic syndrome

ORPHA:314950Заболевание

Primary hypergonadotropic hypogonadism-partial alopecia syndrome

ORPHA:2232Заболевание
Autosomal recessive

Primary hyperoxaluria

ORPHA:416Заболевание
Autosomal recessive