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