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База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы
Найдено 303 заболеваний (Морф.) Сброс

Isolated Dandy-Walker malformation

ORPHA:217Морф.
Multigenic/multifactorial

Isolated absence of upper arm and forearm with hand present

ORPHA:294975Морф.

Isolated absence/hypoplasia of fingers excluding thumb, unilateral

ORPHA:973Морф.
Autosomal dominant, Not applicable

Isolated acheiropodia

ORPHA:931Морф.
Autosomal recessive

Isolated agenesis of gallbladder

ORPHA:440987Морф.
Not applicable

Isolated amyelia

ORPHA:268868Морф.

Isolated anal canal duplication

ORPHA:684752Морф.

Isolated anencephaly/exencephaly

ORPHA:1048Морф.
Multigenic/multifactorial, Not applicable

Isolated aniridia

ORPHA:250923Морф.
Autosomal dominant, Not applicable

Isolated ankyloblepharon filiforme adnatum

ORPHA:91397Морф.
Autosomal dominant, Not applicable

Isolated arhinencephaly

ORPHA:268936Морф.

Isolated bilateral hemispheric cerebellar hypoplasia

ORPHA:269221Морф.

Isolated biliary atresia

ORPHA:30391Морф.
Multigenic/multifactorial

Isolated cerebellar agenesis

ORPHA:1398Морф.

Isolated cerebellar vermis agenesis

ORPHA:269203Морф.

Isolated cleft lip

ORPHA:199302Морф.
Multigenic/multifactorial

Isolated colonic duplication

ORPHA:662392Морф.
Not applicable

Isolated congenital breast hypoplasia/aplasia

ORPHA:180188Морф.
Autosomal recessive

Isolated congenital cholesteatoma of the middle ear

ORPHA:686556Морф.
Unknown

Isolated congenital hypoglossia/aglossia

ORPHA:141152Морф.

Isolated congenital megalocornea

ORPHA:91489Морф.
X-linked recessive

Isolated congenital sclerocornea

ORPHA:91490Морф.
Autosomal dominant

Isolated corpus callosum agenesis

ORPHA:200Морф.
Not applicable

Isolated cryptophthalmia

ORPHA:91396Морф.
Autosomal dominant, Autosomal recessive