MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Lethal neonatal spasticity-epileptic encephalopathy syndrome

ORPHA:435845Malf.
Autosomal recessive

Lethal occipital encephalocele-skeletal dysplasia syndrome

ORPHA:293925Malf.
Autosomal recessive

Lethal omphalocele-cleft palate syndrome

ORPHA:2736Malf.
Autosomal recessive

Lethal polymalformative syndrome, Boissel type

ORPHA:210144Malf.
Autosomal recessive

Lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome

ORPHA:615954Clinical syndrome

Lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to a point mutation

ORPHA:615983Ätl. subt.
Autosomal recessive

Lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to biallelic deletions in the ATAD3 gene cluster

ORPHA:615986Ätl. subt.

Lethal recessive chondrodysplasia

ORPHA:1423Malf.
Autosomal recessive

Letrozole toxicity

ORPHA:529831spez. Sit.

Leukocyte adhesion deficiency

ORPHA:2968Kr.
Autosomal recessive

Leukocyte adhesion deficiency type I

ORPHA:99842Kl. subt.
Autosomal recessive

Leukocyte adhesion deficiency type II

ORPHA:99843Kl. subt.
Autosomal recessive

Leukocyte adhesion deficiency type III

ORPHA:99844Kl. subt.
Autosomal recessive

Leukoencephalopathy with bilateral anterior temporal lobe cysts

ORPHA:139444Kr.
Unknown

Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome

ORPHA:137898Kr.
Autosomal recessive

Leukoencephalopathy with calcifications and cysts

ORPHA:542310Kr.
Autosomal recessive

Leukoencephalopathy with mild cerebellar ataxia and white matter edema

ORPHA:363540Kr.
Autosomal recessive

Leukoencephalopathy-dystonia-motor neuropathy syndrome

ORPHA:163684Kr.
Autosomal recessive

Leukoencephalopathy-palmoplantar keratoderma syndrome

ORPHA:2386Kr.
Autosomal recessive

Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome

ORPHA:83629Kr.
X-linked recessive

Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome

ORPHA:314051Kr.
No data available

Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome

ORPHA:1816Malf.
Autosomal recessive

Leukonychia totalis

ORPHA:2387Kr.
Autosomal dominant, Autosomal recessive

Leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome

ORPHA:210133Kr.
Autosomal dominant