MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Iatrogenic botulism

ORPHA:254509Kl. subt.

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

Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome

ORPHA:2269Kr.
Autosomal recessive

Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome

ORPHA:2274Kr.
Autosomal recessive, X-linked recessive

Ichthyosis-hypotrichosis syndrome

ORPHA:91132Kr.
Autosomal recessive

Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome

ORPHA:2278Malf.

Ichthyosis-oral and digital anomalies syndrome

ORPHA:2272Malf.
Autosomal recessive

Ichthyosis-prematurity syndrome

ORPHA:88621Kr.
Autosomal recessive

Ichthyosis-short stature-brachydactyly-microspherophakia syndrome

ORPHA:363992Kr.
Autosomal recessive

Idiopathic CD4 lymphocytopenia

ORPHA:228000Bio-An.
Not applicable

Idiopathic achalasia

ORPHA:930Kr.
Autosomal recessive, Not applicable

Idiopathic acute eosinophilic pneumonia

ORPHA:724Kr.
Unknown

Idiopathic acute transverse myelitis

ORPHA:139423Kl. subt.
Not applicable

Idiopathic aplastic anemia

ORPHA:88Kr.
Unknown

Idiopathic bronchiectasis

ORPHA:60033Kr.
Not applicable

Idiopathic camptocormia

ORPHA:1320Morph.
Not applicable

Idiopathic catatonia

ORPHA:648919Kr.

Idiopathic chronic eosinophilic pneumonia

ORPHA:2902Kr.
Not applicable

Idiopathic chronic pancreatitis

ORPHA:700133Kr.
Not applicable

Idiopathic congenital hypothyroidism

ORPHA:95717Kr.

Idiopathic copper-associated cirrhosis

ORPHA:209919Kr.
Unknown

Idiopathic dropped head syndrome

ORPHA:447881Clinical syndrome
Not applicable

Idiopathic ductopenia

ORPHA:480512Kr.