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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Bullous lichen planus

ORPHA:33408Ауру
Autosomal dominant, Not applicable

Bullous pemphigoid

ORPHA:703Ауру
Not applicable

Bullous pyoderma gangrenosum

ORPHA:538869Клин. под.
Multigenic/multifactorial

Burkitt lymphoma

ORPHA:543Ауру
Not applicable

Burn-McKeown syndrome

ORPHA:1200Мальф.
Autosomal recessive

Burning mouth syndrome

ORPHA:353253Ауру

Butterfly-shaped pigment dystrophy

ORPHA:99001Ауру
Autosomal dominant

Böök syndrome

ORPHA:1262Мальф.
Autosomal dominant

C syndrome

ORPHA:1308Мальф.
Not applicable, Unknown

C11ORF73-related autosomal recessive hypomyelinating leukodystrophy

ORPHA:495844Ауру
Autosomal recessive

C12ORF65-related combined oxidative phosphorylation defect

ORPHA:497623Клин. топ

C3 glomerulonephritis

ORPHA:329931Гист. под.
Autosomal dominant

C3 glomerulopathy

ORPHA:329918Клин. под.
Multigenic/multifactorial

CACH syndrome

ORPHA:135Ауру
Autosomal recessive

CAD-CDG

ORPHA:448010Ауру
Autosomal recessive

CADDS

ORPHA:369942Ауру
X-linked recessive

CADINS disease

ORPHA:619972Ауру
Autosomal dominant

CAMOS syndrome

ORPHA:83472Мальф.
Autosomal recessive

CANOMAD syndrome

ORPHA:71279Ауру

CAR T cell therapy-associated cytokine release syndrome

ORPHA:542323Жағдай

CARD8-related inflammatory bowel disease

ORPHA:714410Ауру
Autosomal dominant

CCDC115-CDG

ORPHA:468684Ауру
Autosomal recessive

CCNK-related neurodevelopmental disorder-severe intellectual disability-facial dysmorphism syndrome

ORPHA:600668Ауру
Autosomal dominant

CDK13-related developmental delay-intellectual disability-facial dysmorphism-congenital heart defects syndrome

ORPHA:646278Ауру
Autosomal dominant