MEDLIB
База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

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

Isolated cryptophthalmia

ORPHA:91396Морф.
Autosomal dominant, Autosomal recessive

Isolated cytochrome C oxidase deficiency

ORPHA:254905Заболевание
Autosomal recessive, Mitochondrial inheritance

Isolated delta-storage pool disease

ORPHA:248340Заболевание
Autosomal dominant, Autosomal recessive

Isolated distal symphalangism

ORPHA:3248Морф.
Autosomal dominant

Isolated duodenal duplication

ORPHA:662473Клин. подт.
Not applicable

Isolated ectopia lentis

ORPHA:1885Порок
Autosomal dominant, Autosomal recessive

Isolated epispadias

ORPHA:93928Клин. подт.
Multigenic/multifactorial

Isolated exencephaly

ORPHA:563612Клин. подт.

Isolated familial medullary thyroid carcinoma

ORPHA:99361Заболевание
Autosomal dominant

Isolated female hypospadias

ORPHA:603515Морф.

Isolated femoral agenesis/hypoplasia

ORPHA:1987Морф.

Isolated fibular hemimelia

ORPHA:93323Морф.
Not applicable

Isolated focal cortical dysplasia

ORPHA:65683Заболевание

Isolated focal cortical dysplasia type I

ORPHA:268961Клин. подт.

Isolated focal cortical dysplasia type II

ORPHA:268994Клин. подт.

Isolated focal cortical dysplasia type IIa

ORPHA:269001Гист. подт.
Not applicable

Isolated focal cortical dysplasia type IIb

ORPHA:269008Гист. подт.
Not applicable

Isolated focal cortical dysplasia type Ia

ORPHA:268973Гист. подт.
Not applicable

Isolated focal cortical dysplasia type Ib

ORPHA:268980Гист. подт.

Isolated focal cortical dysplasia type Ic

ORPHA:268987Гист. подт.

Isolated focal non-epidermolytic palmoplantar keratoderma

ORPHA:448264Заболевание
Autosomal dominant

Isolated follicle stimulating hormone deficiency

ORPHA:52901Заболевание
Autosomal recessive

Isolated gallbladder duplication

ORPHA:662388Морф.
Not applicable

Isolated gastric duplication

ORPHA:662376Морф.
Not applicable