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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Isolated neonatal sclerosing cholangitis

ORPHA:480556Ауру
Autosomal recessive

Isolated optic nerve aplasia

ORPHA:637064Морф.

Isolated optic nerve hypoplasia

ORPHA:637061Морф.

Isolated osteopoikilosis

ORPHA:166119Ауру
Autosomal dominant

Isolated partial cerebellar vermis agenesis

ORPHA:269209Клин. под.

Isolated partial vaginal agenesis

ORPHA:96269Морф.

Isolated patella aplasia/hypoplasia

ORPHA:86789Морф.
Autosomal dominant

Isolated permanent neonatal diabetes mellitus

ORPHA:99885Ауру
Autosomal dominant, Autosomal recessive

Isolated polycystic liver disease

ORPHA:2924Мальф.
Autosomal dominant, Not applicable

Isolated posterior meningocele

ORPHA:268810Морф.
Multigenic/multifactorial, Not applicable

Isolated primary pigmented nodular adrenocortical disease

ORPHA:647772Ауру

Isolated proximal femoral focal deficiency

ORPHA:633228Морф.

Isolated pulmonary capillaritis

ORPHA:264691Ауру
Not applicable

Isolated punctate palmoplantar keratoderma

ORPHA:2338Клин. топ
Autosomal dominant

Isolated pyloric duplication

ORPHA:662405Морф.
Not applicable

Isolated radial hemimelia

ORPHA:93321Морф.
Multigenic/multifactorial, X-linked recessive

Isolated radio-ulnar synostosis

ORPHA:3269Морф.
Unknown

Isolated rare lymphatic malformation

ORPHA:2415Сан.
Not applicable

Isolated right ventricular hypoplasia

ORPHA:439Морф.
Autosomal recessive, Not applicable

Isolated sedoheptulokinase deficiency

ORPHA:440713Ауру
Autosomal recessive

Isolated small intestine duplication

ORPHA:662456Морф.
Not applicable

Isolated splenic vein thrombosis

ORPHA:583856Ауру

Isolated splenogonadal fusion

ORPHA:457083Морф.
No data available

Isolated split hand-split foot malformation

ORPHA:2440Мальф.
Autosomal dominant, Autosomal recessive, X-linked recessive