MEDLIB
База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Isolated cryptophthalmia

ORPHA:91396Morph.
Autosomal dominant, Autosomal recessive

Isolated cytochrome C oxidase deficiency

ORPHA:254905Disease
Autosomal recessive, Mitochondrial inheritance

Isolated delta-storage pool disease

ORPHA:248340Disease
Autosomal dominant, Autosomal recessive

Isolated distal symphalangism

ORPHA:3248Morph.
Autosomal dominant

Isolated duodenal duplication

ORPHA:662473Clin. sub.
Not applicable

Isolated ectopia lentis

ORPHA:1885Malform.
Autosomal dominant, Autosomal recessive

Isolated epispadias

ORPHA:93928Clin. sub.
Multigenic/multifactorial

Isolated exencephaly

ORPHA:563612Clin. sub.

Isolated familial medullary thyroid carcinoma

ORPHA:99361Disease
Autosomal dominant

Isolated female hypospadias

ORPHA:603515Morph.

Isolated femoral agenesis/hypoplasia

ORPHA:1987Morph.

Isolated fibular hemimelia

ORPHA:93323Morph.
Not applicable

Isolated focal cortical dysplasia

ORPHA:65683Disease

Isolated focal cortical dysplasia type I

ORPHA:268961Clin. sub.

Isolated focal cortical dysplasia type II

ORPHA:268994Clin. sub.

Isolated focal cortical dysplasia type IIa

ORPHA:269001Hist. sub.
Not applicable

Isolated focal cortical dysplasia type IIb

ORPHA:269008Hist. sub.
Not applicable

Isolated focal cortical dysplasia type Ia

ORPHA:268973Hist. sub.
Not applicable

Isolated focal cortical dysplasia type Ib

ORPHA:268980Hist. sub.

Isolated focal cortical dysplasia type Ic

ORPHA:268987Hist. sub.

Isolated focal non-epidermolytic palmoplantar keratoderma

ORPHA:448264Disease
Autosomal dominant

Isolated follicle stimulating hormone deficiency

ORPHA:52901Disease
Autosomal recessive

Isolated gallbladder duplication

ORPHA:662388Morph.
Not applicable

Isolated gastric duplication

ORPHA:662376Morph.
Not applicable