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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Neuronal intranuclear inclusion disease

ORPHA:2289Ауру
Autosomal dominant

Neurooculocardiogenitourinary syndrome

ORPHA:684305Ауру
Autosomal dominant

Neuropathy with hearing impairment

ORPHA:139512Ауру
Autosomal dominant

Neurotrophic keratopathy

ORPHA:137596Ауру
Not applicable

Neurovascular malformation

ORPHA:102006Сан.

Neutral lipid storage disease

ORPHA:165Клин. топ
Autosomal recessive

Neutral lipid storage disease with ichthyosis

ORPHA:98907Ауру
Autosomal recessive

Neutral lipid storage disease with myopathy

ORPHA:98908Ауру
Autosomal recessive

Neutropenia-monocytopenia-deafness syndrome

ORPHA:2690Ауру
Unknown

Nevus comedonicus syndrome

ORPHA:64754Ауру
Not applicable

Nevus of Ito

ORPHA:263432Ауру
Not applicable

Nevus of Ota

ORPHA:263425Ауру
Not applicable

New-onset refractory status epilepticus

ORPHA:363558Ауру

Nicolaides-Baraitser syndrome

ORPHA:3051Мальф.
Autosomal dominant

Nicolau syndrome

ORPHA:664787Clinical syndrome

Niemann-Pick disease type C

ORPHA:646Ауру
Autosomal recessive

Niemann-Pick disease type C, adult neurologic onset

ORPHA:216986Клин. под.
Autosomal recessive

Niemann-Pick disease type C, juvenile neurologic onset

ORPHA:216981Клин. под.
Autosomal recessive

Niemann-Pick disease type C, late infantile neurologic onset

ORPHA:216978Клин. под.
Autosomal recessive

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

ORPHA:216975Клин. под.
Autosomal recessive

Niemann-Pick disease type C, severe perinatal form

ORPHA:216972Клин. под.
Autosomal recessive

Night blindness-skeletal anomalies-dysmorphism syndrome

ORPHA:1390Мальф.

Nijmegen breakage syndrome

ORPHA:647Мальф.
Autosomal recessive

Nijmegen breakage syndrome-like disorder

ORPHA:240760Мальф.
Autosomal recessive