MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Neuronal intranuclear inclusion disease

ORPHA:2289Kr.
Autosomal dominant

Neurooculocardiogenitourinary syndrome

ORPHA:684305Kr.
Autosomal dominant

Neuropathy with hearing impairment

ORPHA:139512Kr.
Autosomal dominant

Neurotrophic keratopathy

ORPHA:137596Kr.
Not applicable

Neurovascular malformation

ORPHA:102006Kat.

Neutral lipid storage disease

ORPHA:165Kl. gruppe
Autosomal recessive

Neutral lipid storage disease with ichthyosis

ORPHA:98907Kr.
Autosomal recessive

Neutral lipid storage disease with myopathy

ORPHA:98908Kr.
Autosomal recessive

Neutropenia-monocytopenia-deafness syndrome

ORPHA:2690Kr.
Unknown

Nevus comedonicus syndrome

ORPHA:64754Kr.
Not applicable

Nevus of Ito

ORPHA:263432Kr.
Not applicable

Nevus of Ota

ORPHA:263425Kr.
Not applicable

New-onset refractory status epilepticus

ORPHA:363558Kr.

Nicolaides-Baraitser syndrome

ORPHA:3051Malf.
Autosomal dominant

Nicolau syndrome

ORPHA:664787Clinical syndrome

Niemann-Pick disease type C

ORPHA:646Kr.
Autosomal recessive

Niemann-Pick disease type C, adult neurologic onset

ORPHA:216986Kl. subt.
Autosomal recessive

Niemann-Pick disease type C, juvenile neurologic onset

ORPHA:216981Kl. subt.
Autosomal recessive

Niemann-Pick disease type C, late infantile neurologic onset

ORPHA:216978Kl. subt.
Autosomal recessive

Niemann-Pick disease type C, severe early infantile neurologic onset

ORPHA:216975Kl. subt.
Autosomal recessive

Niemann-Pick disease type C, severe perinatal form

ORPHA:216972Kl. subt.
Autosomal recessive

Night blindness-skeletal anomalies-dysmorphism syndrome

ORPHA:1390Malf.

Nijmegen breakage syndrome

ORPHA:647Malf.
Autosomal recessive

Nijmegen breakage syndrome-like disorder

ORPHA:240760Malf.
Autosomal recessive