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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы
Найдено 218 заболеваний (Клин. гр.) Сброс

Müllerian aplasia

ORPHA:73217Клин. гр.
Autosomal dominant

NLRP3-associated autoinflammatory disease

ORPHA:208650Клин. гр.
Autosomal dominant, Not applicable

Nemaline myopathy

ORPHA:607Клин. гр.
Autosomal dominant, Autosomal recessive, Not applicable

Neuroacanthocytosis

ORPHA:263440Клин. гр.

Neurodegeneration with brain iron accumulation

ORPHA:385Клин. гр.
Autosomal dominant, Autosomal recessive, X-linked dominant

Neuronal ceroid lipofuscinosis

ORPHA:216Клин. гр.
Autosomal dominant, Autosomal recessive

Neutral lipid storage disease

ORPHA:165Клин. гр.
Autosomal recessive

Non-histaminic angioedema

ORPHA:658Клин. гр.
Autosomal dominant, Not applicable

Non-rhizomelic chondrodysplasia punctata

ORPHA:176Клин. гр.
Autosomal dominant, Autosomal recessive, X-linked dominant, X-linked recessive

Non-syndromic anorectal malformation

ORPHA:557Клин. гр.

Non-syndromic craniosynostosis

ORPHA:139390Клин. гр.

Non-syndromic hemimelia

ORPHA:2130Клин. гр.
Not applicable

Non-syndromic pontocerebellar hypoplasia

ORPHA:98523Клин. гр.
Autosomal recessive

Oblique facial cleft

ORPHA:141253Клин. гр.

Oculocutaneous albinism

ORPHA:55Клин. гр.
Autosomal recessive

Oligoastrocytic tumor

ORPHA:251651Клин. гр.

Oligodendroglial tumor

ORPHA:46484Клин. гр.
Multigenic/multifactorial, Not applicable

Open spinal dysraphism

ORPHA:268369Клин. гр.
Multigenic/multifactorial, Not applicable

Oromandibular-limb hypogenesis syndrome

ORPHA:2749Клин. гр.

Osteopetrosis and related disorders

ORPHA:2781Клин. гр.
Autosomal dominant, Autosomal recessive, X-linked recessive

Paramedian facial cleft

ORPHA:155867Клин. гр.

Paroxysmal dyskinesia

ORPHA:1431Клин. гр.
Autosomal dominant, Not applicable

Peeling skin syndrome

ORPHA:817Клин. гр.
Autosomal recessive

Peroxisome biogenesis disorder

ORPHA:79189Клин. гр.
Autosomal recessive