MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Neuronal intranuclear inclusion disease

ORPHA:2289Заболевание
Autosomal dominant

Neurooculocardiogenitourinary syndrome

ORPHA:684305Заболевание
Autosomal dominant

Neuropathy with hearing impairment

ORPHA:139512Заболевание
Autosomal dominant

Neurotrophic keratopathy

ORPHA:137596Заболевание
Not applicable

Neurovascular malformation

ORPHA:102006Категория

Neutral lipid storage disease

ORPHA:165Клин. группа
Autosomal recessive

Neutral lipid storage disease with ichthyosis

ORPHA:98907Заболевание
Autosomal recessive

Neutral lipid storage disease with myopathy

ORPHA:98908Заболевание
Autosomal recessive

Neutropenia-monocytopenia-deafness syndrome

ORPHA:2690Заболевание
Unknown

Nevus comedonicus syndrome

ORPHA:64754Заболевание
Not applicable

Nevus of Ito

ORPHA:263432Заболевание
Not applicable

Nevus of Ota

ORPHA:263425Заболевание
Not applicable

New-onset refractory status epilepticus

ORPHA:363558Заболевание

Nicolaides-Baraitser syndrome

ORPHA:3051Мальформация
Autosomal dominant

Nicolau syndrome

ORPHA:664787Clinical syndrome

Niemann-Pick disease type C

ORPHA:646Заболевание
Autosomal recessive

Niemann-Pick disease type C, adult neurologic onset

ORPHA:216986Клин. подтип
Autosomal recessive

Niemann-Pick disease type C, juvenile neurologic onset

ORPHA:216981Клин. подтип
Autosomal recessive

Niemann-Pick disease type C, late infantile neurologic onset

ORPHA:216978Клин. подтип
Autosomal recessive

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

ORPHA:216975Клин. подтип
Autosomal recessive

Niemann-Pick disease type C, severe perinatal form

ORPHA:216972Клин. подтип
Autosomal recessive

Night blindness-skeletal anomalies-dysmorphism syndrome

ORPHA:1390Мальформация

Nijmegen breakage syndrome

ORPHA:647Мальформация
Autosomal recessive

Nijmegen breakage syndrome-like disorder

ORPHA:240760Мальформация
Autosomal recessive