MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов
Найдено 3,968 заболеваний (Заболевание)Сбросить

Hypothyroidism due to deficient transcription factors involved in pituitary development or function

ORPHA:226307Заболевание
Autosomal dominant, Autosomal recessive

Hypotonia with lactic acidemia and hyperammonemia

ORPHA:137908Заболевание
Autosomal recessive

Hypotonia-cystinuria syndrome

ORPHA:163690Заболевание
Autosomal recessive

Hypotonia-failure to thrive-microcephaly syndrome

ORPHA:79507Заболевание
Autosomal recessive

Hypotonia-speech impairment-severe cognitive delay syndrome

ORPHA:371364Заболевание
Autosomal recessive

Hypotrichosis simplex

ORPHA:55654Заболевание
Autosomal dominant, Autosomal recessive

Hypotrichosis simplex of the scalp

ORPHA:90368Заболевание
Autosomal dominant

Hypotrichosis-deafness syndrome

ORPHA:330029Заболевание
Autosomal dominant

Hypotrichosis-intellectual disability, Lopes type

ORPHA:2266Заболевание
Autosomal recessive

Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome

ORPHA:69735Заболевание
Autosomal dominant, Autosomal recessive

Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome

ORPHA:307936Заболевание

Hypoxanthine guanine phosphoribosyltransferase partial deficiency

ORPHA:79233Заболевание
X-linked recessive

ICHAD syndrome

ORPHA:699599Заболевание
Autosomal dominant

IFIH1-related hereditary spastic paraplegia

ORPHA:689231Заболевание
Autosomal dominant

IL21-related infantile inflammatory bowel disease

ORPHA:477661Заболевание
Autosomal recessive

IRF2BPL-related regressive neurodevelopmental disorder-dystonia-seizures syndrome

ORPHA:597623Заболевание
Autosomal dominant

IRIDA syndrome

ORPHA:209981Заболевание
Autosomal recessive

IRVAN syndrome

ORPHA:209943Заболевание
Not applicable

ISPD-related limb-girdle muscular dystrophy R20

ORPHA:352479Заболевание
Autosomal recessive

ITM2B amyloidosis

ORPHA:439254Заболевание
Autosomal dominant

ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement

ORPHA:457375Заболевание
Autosomal recessive

Iatrogenic Creutzfeldt-Jakob disease

ORPHA:576379Заболевание

Ichthyosis follicularis-alopecia-photophobia syndrome

ORPHA:2273Заболевание
Autosomal dominant, Not applicable, X-linked recessive

Ichthyosis hystrix of Curth-Macklin

ORPHA:79503Заболевание
Autosomal dominant, Not applicable