MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Lissencephaly with cerebellar hypoplasia

ORPHA:86823Kl. gruppe

Lissencephaly with cerebellar hypoplasia type A

ORPHA:100011Malf.

Lissencephaly with cerebellar hypoplasia type B

ORPHA:100012Malf.

Lissencephaly with cerebellar hypoplasia type C

ORPHA:100013Malf.

Lissencephaly with cerebellar hypoplasia type D

ORPHA:100014Malf.

Lissencephaly with cerebellar hypoplasia type E

ORPHA:100015Malf.

Lissencephaly with cerebellar hypoplasia type F

ORPHA:100016Malf.

Listeriosis

ORPHA:533Kr.
Not applicable

Livedoid vasculopathy

ORPHA:542643Clinical syndrome

Liver adenomatosis

ORPHA:566841Kr.

Lobar holoprosencephaly

ORPHA:93924Kl. subt.
Multigenic/multifactorial, Not applicable

Localized dystrophic epidermolysis bullosa

ORPHA:595356Kr.
Autosomal dominant, Autosomal recessive

Localized dystrophic epidermolysis bullosa, acral form

ORPHA:158673Kl. subt.
Autosomal dominant, Autosomal recessive

Localized dystrophic epidermolysis bullosa, nails only

ORPHA:158676Kl. subt.
Autosomal dominant, Autosomal recessive

Localized dystrophic epidermolysis bullosa, pretibial form

ORPHA:79410Kl. subt.
Autosomal dominant, Autosomal recessive

Localized epidermolysis bullosa simplex

ORPHA:79400Kr.
Autosomal dominant

Localized junctional epidermolysis bullosa

ORPHA:251393Kr.
Autosomal recessive

Localized lichen myxedematosus with mixed features of different subtypes

ORPHA:90398Kl. subt.

Localized lichen myxedematosus with monoclonal gammopathy or systemic symptoms

ORPHA:90399Kl. subt.

Localized lipodystrophy

ORPHA:79088Kl. gruppe
Unknown

Localized pagetoid reticulosis

ORPHA:178517Kr.
Not applicable

Localized scleroderma

ORPHA:90289Kr.
Not applicable

Locked-in syndrome

ORPHA:2406Clinical syndrome
Not applicable

Loeffler endocarditis

ORPHA:75566Kr.