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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Agammaglobulinemia-early-onset hypertrophic cardiomyopathy-neutropenia syndrome

ORPHA:693647Ауру
Autosomal recessive

Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome

ORPHA:83617Мальф.
Autosomal recessive

Agammaglobulinemia-skin involvement-failure to thrive syndrome

ORPHA:693627Ауру
Autosomal recessive

Aggressive B-cell non-Hodgkin lymphoma

ORPHA:300846Сан.

Aggressive NK-cell leukemia

ORPHA:86873Ауру
Multigenic/multifactorial, Not applicable

Aggressive periodontitis

ORPHA:447740Ауру
Autosomal recessive

Aggressive systemic mastocytosis

ORPHA:98850Ауру
Not applicable

Agnathia-holoprosencephaly-situs inversus syndrome

ORPHA:990Мальф.
Autosomal dominant, Autosomal recessive, Not applicable

Aicardi syndrome

ORPHA:50Ауру
X-linked dominant

Aicardi-Goutières syndrome

ORPHA:51Ауру
Autosomal dominant, Autosomal recessive

Airway infantile hemangioma

ORPHA:137935Ауру
Not applicable

Alacrimia-choreoathetosis-liver dysfunction syndrome

ORPHA:404454Ауру
Autosomal recessive

Alagille syndrome

ORPHA:52Мальф.
Autosomal dominant

Alagille syndrome due to 20p12 microdeletion

ORPHA:261600Этио. под.
Not applicable

Alagille syndrome due to a JAG1 point mutation

ORPHA:261619Этио. под.
Autosomal dominant

Alagille syndrome due to a NOTCH2 point mutation

ORPHA:261629Этио. под.
Autosomal dominant

Alar cartilages hypoplasia-coloboma-telecanthus syndrome

ORPHA:2007Мальф.
Autosomal recessive

Alazami syndrome

ORPHA:319671Мальф.
Autosomal recessive

Alazami-Yuan syndrome

ORPHA:694946Мальф.
Autosomal recessive

Albers-Schönberg osteopetrosis

ORPHA:53Мальф.
Autosomal dominant

Albinism-deafness syndrome

ORPHA:998Мальф.
X-linked recessive

Alexander disease

ORPHA:58Ауру
Autosomal dominant

Alexander disease type I

ORPHA:363717Клин. под.
Not applicable

Alexander disease type II

ORPHA:363722Клин. под.
Autosomal dominant