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Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Congenital glucokinase-related hyperinsulinism

ORPHA:79299Ауру
Autosomal dominant

Congenital heart block

ORPHA:60041Ауру
Not applicable

Congenital heart defect-ectodermal dysplasia- brachydactyly-telangiectasia syndrome

ORPHA:708019Мальф.
Autosomal dominant

Congenital heart defect-round face-developmental delay syndrome

ORPHA:1355Мальф.

Congenital hereditary endothelial dystrophy type II

ORPHA:293603Ауру
Autosomal recessive

Congenital hereditary facial paralysis-variable hearing loss syndrome

ORPHA:306530Морф.
Autosomal recessive

Congenital herpes simplex virus infection

ORPHA:293Ауру
Not applicable

Congenital high-molecular-weight kininogen deficiency

ORPHA:483Ауру
Autosomal recessive

Congenital hydrocephalus

ORPHA:2185Мальф.
Not applicable

Congenital hyperinsulinism due to HNF4A deficiency

ORPHA:263455Ауру
Autosomal dominant

Congenital hypogonadotropic hypogonadism

ORPHA:174590Сан.
Autosomal dominant, Autosomal recessive, X-linked recessive

Congenital hypothyroidism

ORPHA:442Сан.
Autosomal recessive

Congenital hypothyroidism due to developmental anomaly

ORPHA:95711Сан.

Congenital hypothyroidism due to maternal intake of antithyroid drugs

ORPHA:226313Ауру

Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies

ORPHA:95715Ауру
Not applicable

Congenital ichthyosiform erythroderma

ORPHA:79394Ауру
Autosomal recessive

Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome

ORPHA:352333Ауру
Autosomal recessive

Congenital ichthyosis-microcephalus-tetraplegia syndrome

ORPHA:2271Ауру
Unknown

Congenital infiltrating lipomatosis of the face

ORPHA:583097Ауру

Congenital insensitivity to pain syndrome, Marsili type

ORPHA:653728Ауру
Autosomal dominant

Congenital insensitivity to pain with severe intellectual disability

ORPHA:453510Ауру
Autosomal recessive

Congenital insensitivity to pain-anosmia-neuropathic arthropathy

ORPHA:88642Ауру
Autosomal dominant, Autosomal recessive

Congenital insensitivity to pain-hyperhidrosis-absence of cutaneous sensory innervation

ORPHA:217399Ауру
Unknown

Congenital intrahepatic arterioportal fistula

ORPHA:694228Мальф.
Not applicable