MEDLIB
База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы

Pili torti-developmental delay-neurological abnormalities syndrome

ORPHA:2891Порок

Pili torti-onychodysplasia syndrome

ORPHA:2890Порок
Autosomal recessive

Pilocytic astrocytoma

ORPHA:251612Заболевание
Not applicable

Pilodental dysplasia-refractive errors syndrome

ORPHA:2892Порок
Autosomal recessive

Pilomatrix carcinoma

ORPHA:499182Заболевание

Pilomatrixoma

ORPHA:91414Заболевание
Not applicable

Pilomyxoid astrocytoma

ORPHA:251615Гист. подт.
Not applicable

Pineoblastoma

ORPHA:251909Заболевание
Not applicable

Pineocytoma

ORPHA:251912Заболевание

Pitt-Hopkins syndrome

ORPHA:2896Порок
Autosomal dominant

Pituicytoma

ORPHA:251623Заболевание
Not applicable

Pituitary apoplexy

ORPHA:95613Заболевание
Not applicable

Pituitary carcinoma

ORPHA:300385Заболевание
Unknown

Pituitary deficiency due to Rathke cleft cysts

ORPHA:91350Заболевание

Pituitary deficiency due to empty sella turcica syndrome

ORPHA:91354Заболевание

Pituitary dermoid and epidermoid cysts

ORPHA:91351Заболевание

Pituitary gigantism

ORPHA:99725Заболевание
Autosomal dominant, X-linked dominant

Pituitary stalk interruption syndrome

ORPHA:95496Морф.
Autosomal dominant, Autosomal recessive, Not applicable

Pityriasis rubra pilaris

ORPHA:2897Заболевание
Autosomal dominant, Not applicable

Placental insufficiency

ORPHA:439167Clinical syndrome
Not applicable

Placental site trophoblastic tumor

ORPHA:99928Заболевание
Not applicable

Plague

ORPHA:707Заболевание

Plaque-form urticaria pigmentosa

ORPHA:158769Клин. подт.
Autosomal dominant, Unknown

Plasma cell leukemia

ORPHA:454714Заболевание
Not applicable