MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

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

ORPHA:226307Kr.
Autosomal dominant, Autosomal recessive

Hypotonia with lactic acidemia and hyperammonemia

ORPHA:137908Kr.
Autosomal recessive

Hypotonia-cystinuria syndrome

ORPHA:163690Kr.
Autosomal recessive

Hypotonia-failure to thrive-microcephaly syndrome

ORPHA:79507Kr.
Autosomal recessive

Hypotonia-speech impairment-severe cognitive delay syndrome

ORPHA:371364Kr.
Autosomal recessive

Hypotrichosis simplex

ORPHA:55654Kr.
Autosomal dominant, Autosomal recessive

Hypotrichosis simplex of the scalp

ORPHA:90368Kr.
Autosomal dominant

Hypotrichosis-deafness syndrome

ORPHA:330029Kr.
Autosomal dominant

Hypotrichosis-intellectual disability, Lopes type

ORPHA:2266Kr.
Autosomal recessive

Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome

ORPHA:69735Kr.
Autosomal dominant, Autosomal recessive

Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome

ORPHA:307936Kr.

Hypoxanthine guanine phosphoribosyltransferase partial deficiency

ORPHA:79233Kr.
X-linked recessive

ICHAD syndrome

ORPHA:699599Kr.
Autosomal dominant

IFIH1-related hereditary spastic paraplegia

ORPHA:689231Kr.
Autosomal dominant

IL21-related infantile inflammatory bowel disease

ORPHA:477661Kr.
Autosomal recessive

IRF2BPL-related regressive neurodevelopmental disorder-dystonia-seizures syndrome

ORPHA:597623Kr.
Autosomal dominant

IRIDA syndrome

ORPHA:209981Kr.
Autosomal recessive

IRVAN syndrome

ORPHA:209943Kr.
Not applicable

ISPD-related limb-girdle muscular dystrophy R20

ORPHA:352479Kr.
Autosomal recessive

ITM2B amyloidosis

ORPHA:439254Kr.
Autosomal dominant

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

ORPHA:457375Kr.
Autosomal recessive

Iatrogenic Creutzfeldt-Jakob disease

ORPHA:576379Kr.

Ichthyosis follicularis-alopecia-photophobia syndrome

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

Ichthyosis hystrix of Curth-Macklin

ORPHA:79503Kr.
Autosomal dominant, Not applicable