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Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер
Табылды 3,968 заболеваний (Ауру) Қалпына келтіру

Reis-Bücklers corneal dystrophy

ORPHA:98961Ауру
Autosomal dominant

Relapsing fever

ORPHA:91547Ауру
Not applicable

Relapsing polychondritis

ORPHA:728Ауру
Unknown

Renal medullary carcinoma

ORPHA:319319Ауру

Renal nutcracker syndrome

ORPHA:71273Ауру
Unknown

Renal tubulopathy-encephalopathy-liver failure syndrome

ORPHA:254902Ауру
Autosomal recessive

Renin-angiotensin-aldosterone system-blocker-induced angioedema

ORPHA:100057Ауру
Multigenic/multifactorial, Not applicable

Resistance to thyroid hormone due to a mutation in thyroid hormone receptor alpha

ORPHA:566231Ауру
Autosomal dominant

Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta

ORPHA:566243Ауру
Autosomal recessive

Resistance to thyrotropin-releasing hormone syndrome

ORPHA:99832Ауру
Autosomal recessive

Respiratory bronchiolitis-interstitial lung disease syndrome

ORPHA:79127Ауру
Not applicable

Restrictive dermopathy

ORPHA:1662Ауру
Autosomal dominant, Autosomal recessive

Reticular dysgenesis

ORPHA:33355Ауру
Autosomal recessive

Reticular dysgenesis-like severe combined immunodeficiency

ORPHA:688543Ауру
Autosomal dominant

Reticular dystrophy of the retinal pigment epithelium

ORPHA:99002Ауру
Autosomal recessive, Unknown

Reticulate acropigmentation of Kitamura

ORPHA:178307Ауру
Autosomal dominant

Retiform hemangioendothelioma

ORPHA:458763Ауру
Not applicable

Retinal capillary malformation

ORPHA:71213Ауру
Autosomal dominant

Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies

ORPHA:397758Ауру
Autosomal dominant

Retinal dystrophy-optic nerve edema-splenomegaly-anhidrosis-migraine headache syndrome

ORPHA:313800Ауру
Autosomal dominant

Retinal macular dystrophy type 2

ORPHA:319640Ауру
Autosomal dominant

Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations

ORPHA:247691Ауру
Autosomal dominant

Retinitis pigmentosa

ORPHA:791Ауру
Autosomal dominant, Autosomal recessive, Mitochondrial inheritance, X-linked recessive

Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome

ORPHA:436245Ауру
Autosomal recessive