MEDLIB
Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Intraneural perineurioma

ORPHA:100003Ауру

Intraocular medulloepithelioma

ORPHA:268139Ауру
Not applicable

Intraoral basal cell carcinoma

ORPHA:667678Ауру
Not yet documented

Intrauterine growth restriction-congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome

ORPHA:508512Ауру
Autosomal recessive

Intrauterine growth restriction-short stature-early adult-onset diabetes syndrome

ORPHA:436144Ауру
Autosomal dominant

Intrauterine growth retardation-micrognathia-short stature-facial dysmorphism-rhizomelic shortening syndrome

ORPHA:659702Мальф.

Intravascular large B-cell lymphoma

ORPHA:98839Ауру
Not applicable

Invasive candidiasis

ORPHA:636945Ауру

Invasive infections due to vancomycin-resistant enterococci

ORPHA:90078Жағдай

Invasive mole

ORPHA:99925Ауру
Not applicable

Invasive non-typhoidal salmonellosis

ORPHA:324648Ауру

Invasive scopulariopsis infection

ORPHA:633124Ауру

Inverted duplicated chromosome 15 syndrome

ORPHA:3306Мальф.
Not applicable, Unknown

Iridocorneal endothelial syndrome

ORPHA:64734Ауру
Not applicable

Isaacs syndrome

ORPHA:84142Ауру
Not applicable

Isobutyryl-CoA dehydrogenase deficiency

ORPHA:79159Ауру
Autosomal recessive

Isochromosomy Yp syndrome

ORPHA:98797Мальф.

Isochromosomy Yq syndrome

ORPHA:98798Мальф.

Isolated ATP synthase deficiency

ORPHA:254913Ауру
Autosomal recessive

Isolated Dandy-Walker malformation

ORPHA:217Морф.
Multigenic/multifactorial

Isolated Dandy-Walker malformation with hydrocephalus

ORPHA:269212Клин. под.

Isolated Dandy-Walker malformation without hydrocephalus

ORPHA:269215Клин. под.
Multigenic/multifactorial

Isolated Joubert syndrome

ORPHA:475Мальф.
Autosomal recessive

Isolated Klippel-Feil syndrome

ORPHA:2345Мальф.
Autosomal dominant, Autosomal recessive, Not applicable