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Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Spastic paraplegia type 2

ORPHA:99015Ауру
X-linked recessive

Spastic paraplegia type 7

ORPHA:99013Ауру
Autosomal dominant, Autosomal recessive

Spastic paraplegia-Paget disease of bone syndrome

ORPHA:329475Ауру
Autosomal dominant

Spastic paraplegia-facial-cutaneous lesions syndrome

ORPHA:2819Мальф.

Spastic paraplegia-glaucoma-intellectual disability syndrome

ORPHA:2818Ауру
Autosomal recessive

Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome

ORPHA:521390Мальф.
Autosomal dominant

Spastic paraplegia-nephritis-deafness syndrome

ORPHA:2820Clinical syndrome
Autosomal dominant

Spastic paraplegia-neuropathy-poikiloderma syndrome

ORPHA:2821Ауру

Spastic paraplegia-optic atrophy-neuropathy syndrome

ORPHA:320406Ауру
Autosomal recessive

Spastic paraplegia-precocious puberty syndrome

ORPHA:2826Ауру
Autosomal dominant

Spastic paraplegia-severe developmental delay-epilepsy syndrome

ORPHA:464282Ауру
Autosomal recessive

Spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome

ORPHA:3011Ауру
Autosomal recessive

Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome

ORPHA:447997Ауру
Autosomal recessive

Spectrin-associated autosomal recessive cerebellar ataxia

ORPHA:352403Ауру
Autosomal recessive

Spermatocytic seminoma

ORPHA:99865Ауру
Unknown

Spheroid body myopathy

ORPHA:268129Ауру
Autosomal dominant

Spigelian hernia-cryptorchidism syndrome

ORPHA:314432Мальф.
Not applicable

Spina bifida and other spinal dysraphisms

ORPHA:823Сан.
Multigenic/multifactorial, Not applicable

Spina bifida-hypospadias syndrome

ORPHA:3176Мальф.

Spinal arteriovenous metameric syndrome

ORPHA:53721Мальф.
Not applicable

Spinal atrophy-ophthalmoplegia-pyramidal syndrome

ORPHA:1217Ауру

Spinal cord arteriovenous malformation

ORPHA:715284Морф.
Not applicable

Spinal cord injury

ORPHA:90058Жағдай
Not applicable

Spinal dysraphism with a posterior meningocele

ORPHA:268744Клин. топ
Multigenic/multifactorial, Not applicable