MEDLIB
Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

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

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

ORPHA:226307Ауру
Autosomal dominant, Autosomal recessive

Hypotonia with lactic acidemia and hyperammonemia

ORPHA:137908Ауру
Autosomal recessive

Hypotonia-cystinuria syndrome

ORPHA:163690Ауру
Autosomal recessive

Hypotonia-failure to thrive-microcephaly syndrome

ORPHA:79507Ауру
Autosomal recessive

Hypotonia-speech impairment-severe cognitive delay syndrome

ORPHA:371364Ауру
Autosomal recessive

Hypotrichosis simplex

ORPHA:55654Ауру
Autosomal dominant, Autosomal recessive

Hypotrichosis simplex of the scalp

ORPHA:90368Ауру
Autosomal dominant

Hypotrichosis-deafness syndrome

ORPHA:330029Ауру
Autosomal dominant

Hypotrichosis-intellectual disability, Lopes type

ORPHA:2266Ауру
Autosomal recessive

Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome

ORPHA:69735Ауру
Autosomal dominant, Autosomal recessive

Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome

ORPHA:307936Ауру

Hypoxanthine guanine phosphoribosyltransferase partial deficiency

ORPHA:79233Ауру
X-linked recessive

ICHAD syndrome

ORPHA:699599Ауру
Autosomal dominant

IFIH1-related hereditary spastic paraplegia

ORPHA:689231Ауру
Autosomal dominant

IL21-related infantile inflammatory bowel disease

ORPHA:477661Ауру
Autosomal recessive

IRF2BPL-related regressive neurodevelopmental disorder-dystonia-seizures syndrome

ORPHA:597623Ауру
Autosomal dominant

IRIDA syndrome

ORPHA:209981Ауру
Autosomal recessive

IRVAN syndrome

ORPHA:209943Ауру
Not applicable

ISPD-related limb-girdle muscular dystrophy R20

ORPHA:352479Ауру
Autosomal recessive

ITM2B amyloidosis

ORPHA:439254Ауру
Autosomal dominant

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

ORPHA:457375Ауру
Autosomal recessive

Iatrogenic Creutzfeldt-Jakob disease

ORPHA:576379Ауру

Ichthyosis follicularis-alopecia-photophobia syndrome

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

Ichthyosis hystrix of Curth-Macklin

ORPHA:79503Ауру
Autosomal dominant, Not applicable