MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Acquired factor VII deficiency

ORPHA:599495Disease

Acquired factor X deficiency

ORPHA:599501Disease

Acquired factor XI deficiency

ORPHA:599507Disease

Acquired factor XIII deficiency

ORPHA:599513Disease

Acquired generalized lipodystrophy

ORPHA:79086Disease
Not applicable

Acquired hemophagocytic lymphohistiocytosis associated with malignant disease

ORPHA:158057Situation

Acquired hemophilia A

ORPHA:599480Disease
Not applicable

Acquired hemophilia B

ORPHA:599485Disease
Not applicable

Acquired hypertrichosis lanuginosa

ORPHA:2221Disease
Not applicable

Acquired hypothalamic obesity

ORPHA:689401Disease
Not applicable

Acquired ichthyosis

ORPHA:454Disease
Not applicable

Acquired idiopathic sideroblastic anemia

ORPHA:75564Disease
Not applicable

Acquired intracranial dural arteriovenous fistula

ORPHA:715318Disease
Not applicable

Acquired methemoglobinemia

ORPHA:464453Disease
Not applicable

Acquired monoclonal Ig light chain-associated Fanconi syndrome

ORPHA:91136Disease
Not applicable

Acquired partial lipodystrophy

ORPHA:79087Disease
Multigenic/multifactorial, Not applicable

Acquired pseudoxanthoma elasticum

ORPHA:228247Disease
Not applicable

Acquired purpura fulminans

ORPHA:49566Disease
Not applicable

Acquired schizencephaly

ORPHA:485275Etio. sub.

Acquired secondary polycythemia

ORPHA:238547Cat.
Not applicable

Acquired von Willebrand syndrome

ORPHA:99147Disease
Not applicable

Acral peeling skin syndrome

ORPHA:263534Disease
Autosomal recessive

Acral persistent papular mucinosis

ORPHA:90396Disease

Acral self-healing collodion baby

ORPHA:281127Disease
Autosomal recessive, Unknown