MEDLIB
База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

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

Isolated Dandy-Walker malformation

ORPHA:217Morph.
Multigenic/multifactorial

Isolated absence of upper arm and forearm with hand present

ORPHA:294975Morph.

Isolated absence/hypoplasia of fingers excluding thumb, unilateral

ORPHA:973Morph.
Autosomal dominant, Not applicable

Isolated acheiropodia

ORPHA:931Morph.
Autosomal recessive

Isolated agenesis of gallbladder

ORPHA:440987Morph.
Not applicable

Isolated amyelia

ORPHA:268868Morph.

Isolated anal canal duplication

ORPHA:684752Morph.

Isolated anencephaly/exencephaly

ORPHA:1048Morph.
Multigenic/multifactorial, Not applicable

Isolated aniridia

ORPHA:250923Morph.
Autosomal dominant, Not applicable

Isolated ankyloblepharon filiforme adnatum

ORPHA:91397Morph.
Autosomal dominant, Not applicable

Isolated arhinencephaly

ORPHA:268936Morph.

Isolated bilateral hemispheric cerebellar hypoplasia

ORPHA:269221Morph.

Isolated biliary atresia

ORPHA:30391Morph.
Multigenic/multifactorial

Isolated cerebellar agenesis

ORPHA:1398Morph.

Isolated cerebellar vermis agenesis

ORPHA:269203Morph.

Isolated cleft lip

ORPHA:199302Morph.
Multigenic/multifactorial

Isolated colonic duplication

ORPHA:662392Morph.
Not applicable

Isolated congenital breast hypoplasia/aplasia

ORPHA:180188Morph.
Autosomal recessive

Isolated congenital cholesteatoma of the middle ear

ORPHA:686556Morph.
Unknown

Isolated congenital hypoglossia/aglossia

ORPHA:141152Morph.

Isolated congenital megalocornea

ORPHA:91489Morph.
X-linked recessive

Isolated congenital sclerocornea

ORPHA:91490Morph.
Autosomal dominant

Isolated corpus callosum agenesis

ORPHA:200Morph.
Not applicable

Isolated cryptophthalmia

ORPHA:91396Morph.
Autosomal dominant, Autosomal recessive