MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
3,968 diseases matched (Disease) Reset

Kindler epidermolysis bullosa

ORPHA:2908Disease
Autosomal recessive

Kjellin syndrome

ORPHA:100996Disease
Autosomal recessive

Kleine-Levin syndrome

ORPHA:33543Disease

Kniest dysplasia

ORPHA:485Disease
Autosomal dominant

Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome

ORPHA:2698Disease
Autosomal dominant

Kostmann syndrome

ORPHA:99749Disease
Autosomal recessive

Krabbe disease

ORPHA:487Disease
Autosomal recessive

Kufor-Rakeb syndrome

ORPHA:306674Disease
Autosomal recessive

Kuru

ORPHA:454745Disease
Multigenic/multifactorial, Not applicable

Kyasanur forest disease

ORPHA:319254Disease

Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome

ORPHA:496689Disease
Autosomal recessive

Kyphoscoliotic Ehlers-Danlos syndrome

ORPHA:536545Disease

Kyphosis-lateral tongue atrophy-myofibrillar myopathy syndrome

ORPHA:496686Disease
Autosomal recessive

L-2-hydroxyglutaric aciduria

ORPHA:79314Disease
Autosomal recessive

L-Arginine:glycine amidinotransferase deficiency

ORPHA:35704Disease
Autosomal recessive

LAMA5-related multisystemic syndrome

ORPHA:521450Disease
Autosomal dominant

LCAT deficiency

ORPHA:650Disease
Autosomal recessive

LIG4 syndrome

ORPHA:99812Disease
Autosomal recessive

LIPE-related familial partial lipodystrophy

ORPHA:435660Disease
Autosomal recessive

LMNA-related cardiocutaneous progeria syndrome

ORPHA:363618Disease
Autosomal dominant

La Crosse encephalitis

ORPHA:83483Disease
Not applicable

Lafora disease

ORPHA:501Disease
Autosomal recessive

Laing distal myopathy

ORPHA:59135Disease
Autosomal dominant

Lamb-Shaffer syndrome

ORPHA:530983Disease
Autosomal dominant