MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Lethal neonatal spasticity-epileptic encephalopathy syndrome

ORPHA:435845Malform.
Autosomal recessive

Lethal occipital encephalocele-skeletal dysplasia syndrome

ORPHA:293925Malform.
Autosomal recessive

Lethal omphalocele-cleft palate syndrome

ORPHA:2736Malform.
Autosomal recessive

Lethal polymalformative syndrome, Boissel type

ORPHA:210144Malform.
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:615983Etio. sub.
Autosomal recessive

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

ORPHA:615986Etio. sub.

Lethal recessive chondrodysplasia

ORPHA:1423Malform.
Autosomal recessive

Letrozole toxicity

ORPHA:529831Situation

Leukocyte adhesion deficiency

ORPHA:2968Disease
Autosomal recessive

Leukocyte adhesion deficiency type I

ORPHA:99842Clin. sub.
Autosomal recessive

Leukocyte adhesion deficiency type II

ORPHA:99843Clin. sub.
Autosomal recessive

Leukocyte adhesion deficiency type III

ORPHA:99844Clin. sub.
Autosomal recessive

Leukoencephalopathy with bilateral anterior temporal lobe cysts

ORPHA:139444Disease
Unknown

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

ORPHA:137898Disease
Autosomal recessive

Leukoencephalopathy with calcifications and cysts

ORPHA:542310Disease
Autosomal recessive

Leukoencephalopathy with mild cerebellar ataxia and white matter edema

ORPHA:363540Disease
Autosomal recessive

Leukoencephalopathy-dystonia-motor neuropathy syndrome

ORPHA:163684Disease
Autosomal recessive

Leukoencephalopathy-palmoplantar keratoderma syndrome

ORPHA:2386Disease
Autosomal recessive

Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome

ORPHA:83629Disease
X-linked recessive

Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome

ORPHA:314051Disease
No data available

Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome

ORPHA:1816Malform.
Autosomal recessive

Leukonychia totalis

ORPHA:2387Disease
Autosomal dominant, Autosomal recessive

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

ORPHA:210133Disease
Autosomal dominant