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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Extraskeletal Ewing sarcoma

ORPHA:370334Ауру
Not applicable

Extraskeletal myxoid chondrosarcoma

ORPHA:209916Ауру
Not applicable

Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome

ORPHA:1964Мальф.
Autosomal dominant

Eyebrow duplication-syndactyly syndrome

ORPHA:3172Мальф.
Autosomal recessive

Eyelid sebaceous carcinoma

ORPHA:658590Ауру

F12-associated cold autoinflammatory syndrome

ORPHA:617919Ауру
Autosomal dominant

F12-related hereditary angioedema with normal C1Inh

ORPHA:100054Клин. под.
Autosomal dominant

FADD-related immunodeficiency

ORPHA:306550Ауру
Autosomal recessive

FASTKD2-related infantile mitochondrial encephalomyopathy

ORPHA:166105Ауру
Autosomal recessive

FATCO syndrome

ORPHA:2492Мальф.

FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome

ORPHA:404451Мальф.
Autosomal recessive

FG syndrome type 1

ORPHA:93932Ауру
X-linked recessive

FGFR2-related bent bone dysplasia

ORPHA:313855Ауру
Autosomal dominant

FGFR3-related chondrodysplasia

ORPHA:93420Сан.

FKRP-related limb-girdle muscular dystrophy R9

ORPHA:34515Ауру
Autosomal recessive

FLNA-related X-linked myxomatous valvular dysplasia

ORPHA:555877Морф.
X-linked recessive

FLNC-related handgrip and calf weakness-distal myopathy

ORPHA:63273Ауру
Autosomal dominant

FLOTCH syndrome

ORPHA:2045Ауру

FOXG1 syndrome

ORPHA:561854Ауру

FOXG1 syndrome due to 14q12 microdeletion

ORPHA:261144Клин. под.
Not applicable

FOXG1 syndrome due to intragenic alteration

ORPHA:598164Клин. под.
Autosomal dominant

FOXP1 Syndrome

ORPHA:391372Мальф.
Autosomal dominant

FRAXE intellectual disability

ORPHA:100973Ауру
X-linked recessive

FRAXF syndrome

ORPHA:100974Ауру
Unknown