MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Isolated cryptophthalmia

ORPHA:91396Morph.
Autosomal dominant, Autosomal recessive

Isolated cytochrome C oxidase deficiency

ORPHA:254905Kr.
Autosomal recessive, Mitochondrial inheritance

Isolated delta-storage pool disease

ORPHA:248340Kr.
Autosomal dominant, Autosomal recessive

Isolated distal symphalangism

ORPHA:3248Morph.
Autosomal dominant

Isolated duodenal duplication

ORPHA:662473Kl. subt.
Not applicable

Isolated ectopia lentis

ORPHA:1885Malf.
Autosomal dominant, Autosomal recessive

Isolated epispadias

ORPHA:93928Kl. subt.
Multigenic/multifactorial

Isolated exencephaly

ORPHA:563612Kl. subt.

Isolated familial medullary thyroid carcinoma

ORPHA:99361Kr.
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:65683Kr.

Isolated focal cortical dysplasia type I

ORPHA:268961Kl. subt.

Isolated focal cortical dysplasia type II

ORPHA:268994Kl. subt.

Isolated focal cortical dysplasia type IIa

ORPHA:269001His. subt.
Not applicable

Isolated focal cortical dysplasia type IIb

ORPHA:269008His. subt.
Not applicable

Isolated focal cortical dysplasia type Ia

ORPHA:268973His. subt.
Not applicable

Isolated focal cortical dysplasia type Ib

ORPHA:268980His. subt.

Isolated focal cortical dysplasia type Ic

ORPHA:268987His. subt.

Isolated focal non-epidermolytic palmoplantar keratoderma

ORPHA:448264Kr.
Autosomal dominant

Isolated follicle stimulating hormone deficiency

ORPHA:52901Kr.
Autosomal recessive

Isolated gallbladder duplication

ORPHA:662388Morph.
Not applicable

Isolated gastric duplication

ORPHA:662376Morph.
Not applicable