MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Lennox-Gastaut syndrome

ORPHA:2382Kr.
Autosomal dominant, Multigenic/multifactorial, Not applicable

Lenz-Majewski hyperostotic dysplasia

ORPHA:2658Malf.
Autosomal dominant

Leprosy

ORPHA:548Kr.
Multigenic/multifactorial

Leptospirosis

ORPHA:509Kr.
Not applicable

Leri pleonosteosis

ORPHA:2900Malf.
Autosomal dominant

Lesch-Nyhan syndrome

ORPHA:510Kr.
X-linked recessive

Lethal Kniest-like dysplasia

ORPHA:2347Malf.
Autosomal recessive

Lethal Larsen-like syndrome

ORPHA:2371Malf.
Autosomal recessive

Lethal acantholytic erosive disorder

ORPHA:158687Kr.
Autosomal recessive

Lethal arteriopathy syndrome due to fibulin-4 deficiency

ORPHA:314718Kr.
Autosomal recessive

Lethal ataxia with deafness and optic atrophy

ORPHA:1187Kr.
X-linked recessive

Lethal brain and heart developmental defects

ORPHA:580933Malf.
Autosomal recessive

Lethal congenital contracture syndrome type 1

ORPHA:1486Malf.
Autosomal recessive

Lethal congenital contracture syndrome type 2

ORPHA:137776Malf.
Autosomal recessive

Lethal congenital contracture syndrome type 3

ORPHA:137783Malf.
Autosomal recessive

Lethal faciocardiomelic dysplasia

ORPHA:1972Malf.
Autosomal recessive

Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome

ORPHA:444069Malf.
Autosomal recessive

Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome

ORPHA:439897Malf.
Autosomal recessive

Lethal hemolytic anemia-genital anomalies syndrome

ORPHA:1046Malf.
Unknown

Lethal hydranencephaly-diaphragmatic hernia syndrome

ORPHA:480528Malf.
Autosomal recessive

Lethal infantile mitochondrial myopathy

ORPHA:254857Kr.
Mitochondrial inheritance

Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome

ORPHA:2570Malf.
X-linked recessive

Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome

ORPHA:478049Kr.
Autosomal recessive

Lethal multiple pterygium syndrome

ORPHA:33108Malf.
Autosomal recessive, X-linked recessive