MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Isolated neonatal sclerosing cholangitis

ORPHA:480556Disease
Autosomal recessive

Isolated optic nerve aplasia

ORPHA:637064Morph.

Isolated optic nerve hypoplasia

ORPHA:637061Morph.

Isolated osteopoikilosis

ORPHA:166119Disease
Autosomal dominant

Isolated partial cerebellar vermis agenesis

ORPHA:269209Clin. sub.

Isolated partial vaginal agenesis

ORPHA:96269Morph.

Isolated patella aplasia/hypoplasia

ORPHA:86789Morph.
Autosomal dominant

Isolated permanent neonatal diabetes mellitus

ORPHA:99885Disease
Autosomal dominant, Autosomal recessive

Isolated polycystic liver disease

ORPHA:2924Malform.
Autosomal dominant, Not applicable

Isolated posterior meningocele

ORPHA:268810Morph.
Multigenic/multifactorial, Not applicable

Isolated primary pigmented nodular adrenocortical disease

ORPHA:647772Disease

Isolated proximal femoral focal deficiency

ORPHA:633228Morph.

Isolated pulmonary capillaritis

ORPHA:264691Disease
Not applicable

Isolated punctate palmoplantar keratoderma

ORPHA:2338Clin. grp.
Autosomal dominant

Isolated pyloric duplication

ORPHA:662405Morph.
Not applicable

Isolated radial hemimelia

ORPHA:93321Morph.
Multigenic/multifactorial, X-linked recessive

Isolated radio-ulnar synostosis

ORPHA:3269Morph.
Unknown

Isolated rare lymphatic malformation

ORPHA:2415Cat.
Not applicable

Isolated right ventricular hypoplasia

ORPHA:439Morph.
Autosomal recessive, Not applicable

Isolated sedoheptulokinase deficiency

ORPHA:440713Disease
Autosomal recessive

Isolated small intestine duplication

ORPHA:662456Morph.
Not applicable

Isolated splenic vein thrombosis

ORPHA:583856Disease

Isolated splenogonadal fusion

ORPHA:457083Morph.
No data available

Isolated split hand-split foot malformation

ORPHA:2440Malform.
Autosomal dominant, Autosomal recessive, X-linked recessive