MEDLIB
База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Isolated Pierre Robin sequence

ORPHA:718Malform.
Autosomal dominant, Multigenic/multifactorial, Not applicable, Unknown

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 adrenal medullary hyperplasia

ORPHA:688649Disease
Not applicable

Isolated agenesis of gallbladder

ORPHA:440987Morph.
Not applicable

Isolated amyelia

ORPHA:268868Morph.

Isolated anal canal duplication

ORPHA:684752Morph.

Isolated anencephaly

ORPHA:563609Clin. sub.
Multigenic/multifactorial

Isolated anencephaly/exencephaly

ORPHA:1048Morph.
Multigenic/multifactorial, Not applicable

Isolated angioid streaks

ORPHA:674943Disease

Isolated aniridia

ORPHA:250923Morph.
Autosomal dominant, Not applicable

Isolated ankyloblepharon filiforme adnatum

ORPHA:91397Morph.
Autosomal dominant, Not applicable

Isolated anogenital granulomatosis

ORPHA:692256Disease

Isolated anterior cervical hypertrichosis

ORPHA:3387Disease
Autosomal dominant, Autosomal recessive

Isolated arhinencephaly

ORPHA:268936Morph.

Isolated arrhinia

ORPHA:1134Malform.
Not applicable

Isolated asymptomatic elevation of creatine phosphokinase

ORPHA:206599Bio anom.
Autosomal dominant

Isolated atrial standstill

ORPHA:1344Disease
Autosomal dominant, Not applicable

Isolated autosomal dominant hypomagnesemia, Glaudemans type

ORPHA:199326Disease
Autosomal dominant

Isolated bilateral hemispheric cerebellar hypoplasia

ORPHA:269221Morph.

Isolated biliary atresia

ORPHA:30391Morph.
Multigenic/multifactorial

Isolated bone marrow mastocytosis

ORPHA:158778Disease
Autosomal dominant, Unknown

Isolated cerebellar agenesis

ORPHA:1398Morph.