MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
3,968 diseases matched (Disease) Reset

Cone rod dystrophy-short stature syndrome

ORPHA:653709Disease
Autosomal recessive

Confetti-like macular atrophy

ORPHA:221142Disease

Congenital Epstein-Barr virus infection

ORPHA:70596Disease
Not applicable

Congenital abducens nerve palsy

ORPHA:440233Disease
Not applicable

Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency

ORPHA:90795Disease
Autosomal recessive

Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency

ORPHA:90793Disease
Autosomal recessive

Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency

ORPHA:90791Disease
Autosomal recessive

Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency

ORPHA:95699Disease
Autosomal recessive

Congenital alpha2-antiplasmin deficiency

ORPHA:79Disease
Autosomal recessive

Congenital alveolar capillary dysplasia

ORPHA:210122Disease
Autosomal dominant

Congenital amegakaryocytic thrombocytopenia

ORPHA:3319Disease
Autosomal recessive

Congenital analbuminemia

ORPHA:86816Disease
Autosomal recessive

Congenital atransferrinemia

ORPHA:1195Disease
Autosomal recessive

Congenital autosomal recessive small-platelet thrombocytopenia

ORPHA:566192Disease
Autosomal recessive

Congenital axonal neuropathy with encephalopathy

ORPHA:538101Disease

Congenital bile acid synthesis defect type 1

ORPHA:79301Disease
Autosomal recessive

Congenital bile acid synthesis defect type 2

ORPHA:79303Disease
Autosomal recessive

Congenital bile acid synthesis defect type 3

ORPHA:79302Disease
Autosomal recessive

Congenital bile acid synthesis defect type 4

ORPHA:79095Disease
Autosomal recessive

Congenital brain dysgenesis due to glutamine synthetase deficiency

ORPHA:71278Disease
Autosomal recessive

Congenital cataract-hearing loss-severe developmental delay syndrome

ORPHA:300313Disease
Autosomal recessive

Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome

ORPHA:1369Disease
Autosomal recessive

Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome

ORPHA:330054Disease
Autosomal recessive

Congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome

ORPHA:521432Disease
Autosomal recessive