MEDLIB
База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы

Isolated Pierre Robin sequence

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

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 adrenal medullary hyperplasia

ORPHA:688649Заболевание
Not applicable

Isolated agenesis of gallbladder

ORPHA:440987Морф.
Not applicable

Isolated amyelia

ORPHA:268868Морф.

Isolated anal canal duplication

ORPHA:684752Морф.

Isolated anencephaly

ORPHA:563609Клин. подт.
Multigenic/multifactorial

Isolated anencephaly/exencephaly

ORPHA:1048Морф.
Multigenic/multifactorial, Not applicable

Isolated angioid streaks

ORPHA:674943Заболевание

Isolated aniridia

ORPHA:250923Морф.
Autosomal dominant, Not applicable

Isolated ankyloblepharon filiforme adnatum

ORPHA:91397Морф.
Autosomal dominant, Not applicable

Isolated anogenital granulomatosis

ORPHA:692256Заболевание

Isolated anterior cervical hypertrichosis

ORPHA:3387Заболевание
Autosomal dominant, Autosomal recessive

Isolated arhinencephaly

ORPHA:268936Морф.

Isolated arrhinia

ORPHA:1134Порок
Not applicable

Isolated asymptomatic elevation of creatine phosphokinase

ORPHA:206599Биоаном.
Autosomal dominant

Isolated atrial standstill

ORPHA:1344Заболевание
Autosomal dominant, Not applicable

Isolated autosomal dominant hypomagnesemia, Glaudemans type

ORPHA:199326Заболевание
Autosomal dominant

Isolated bilateral hemispheric cerebellar hypoplasia

ORPHA:269221Морф.

Isolated biliary atresia

ORPHA:30391Морф.
Multigenic/multifactorial

Isolated bone marrow mastocytosis

ORPHA:158778Заболевание
Autosomal dominant, Unknown

Isolated cerebellar agenesis

ORPHA:1398Морф.