MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Early-onset inflammatory bowel disease-ulcerative skin lesions-immunodeficiency syndrome

ORPHA:714477Kr.
Autosomal recessive

Early-onset lamellar cataract

ORPHA:441452Kl. subt.
Autosomal dominant

Early-onset myopathy with fatal cardiomyopathy

ORPHA:289377Kr.
Autosomal recessive

Early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome

ORPHA:439212Kr.
Autosomal recessive

Early-onset nuclear cataract

ORPHA:98991Kl. subt.
Autosomal dominant, Autosomal recessive, X-linked recessive

Early-onset obesity-hyperphagia-severe developmental delay syndrome

ORPHA:99704Kr.
Autosomal dominant

Early-onset parkinsonism-intellectual disability syndrome

ORPHA:2379Kr.
X-linked recessive

Early-onset partial cataract

ORPHA:98992Kl. subt.
Autosomal dominant, Autosomal recessive, X-linked recessive

Early-onset posterior polar cataract

ORPHA:98993Kl. subt.
Autosomal dominant

Early-onset posterior subcapsular cataract

ORPHA:441447Kl. subt.
Autosomal dominant, Autosomal recessive

Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome

ORPHA:496641Malf.
Autosomal recessive

Early-onset progressive encephalopathy with migrant continuous myoclonus

ORPHA:1943Kr.
Unknown

Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome

ORPHA:500144Malf.
Autosomal recessive

Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome

ORPHA:496756Kr.
Autosomal recessive

Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome

ORPHA:3240Kr.
Autosomal recessive

Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome

ORPHA:352654Kr.
Autosomal recessive

Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome

ORPHA:505237Malf.
Autosomal recessive

Early-onset severe Hermansky-Pudlak syndrome with hearing loss, due to AP3D1 deficiency

ORPHA:664511Kl. subt.
Autosomal recessive

Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome

ORPHA:313772Kr.
Autosomal recessive

Early-onset sutural cataract

ORPHA:98985Kl. subt.
Autosomal dominant

Early-onset zonular cataract

ORPHA:98995Kl. subt.
Autosomal dominant, Autosomal recessive, X-linked recessive

East Texas bleeding disorder

ORPHA:391320Ätl. subt.
Autosomal dominant

Eastern equine encephalitis

ORPHA:83594Kr.
Not applicable

Eating reflex epilepsy

ORPHA:166418Kr.