MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
1,772 diseases matched (Malform.) Reset

Jacobsen syndrome

ORPHA:2308Malform.
Not applicable, Unknown

Jalili syndrome

ORPHA:1873Malform.
Autosomal recessive

Jawad syndrome

ORPHA:313795Malform.
Autosomal recessive

Jeune syndrome

ORPHA:474Malform.
Autosomal recessive

Johanson-Blizzard syndrome

ORPHA:2315Malform.
Autosomal recessive

Johnson neuroectodermal syndrome

ORPHA:2316Malform.
Autosomal dominant

Joubert syndrome with Jeune asphyxiating thoracic dystrophy

ORPHA:397715Malform.
Autosomal recessive

Joubert syndrome with ocular defect

ORPHA:220493Malform.
Autosomal recessive

Joubert syndrome with oculorenal defect

ORPHA:2318Malform.
Autosomal recessive

Joubert syndrome with renal defect

ORPHA:220497Malform.
Autosomal recessive

Juberg-Hayward syndrome

ORPHA:2319Malform.
Autosomal dominant, Autosomal recessive

Jung syndrome

ORPHA:2321Malform.

Juvenile Paget disease

ORPHA:2801Malform.
Autosomal recessive

KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome

ORPHA:457193Malform.
Autosomal dominant

KBG syndrome

ORPHA:2332Malform.
Autosomal dominant

KDM5C-related syndromic X-linked intellectual disability

ORPHA:85279Malform.
X-linked recessive

KLHL7-related Bohring-Opitz-like and Crisponi/Cold-induced sweating-like overlap syndrome

ORPHA:603684Malform.
Autosomal recessive

KLHL7-related Bohring-Opitz-like syndrome

ORPHA:603689Malform.
Autosomal recessive

Kabuki syndrome

ORPHA:2322Malform.
Autosomal dominant, Not applicable

Kagami-Ogata syndrome

ORPHA:254519Malform.
Autosomal dominant, Not applicable

Kallmann syndrome-heart disease syndrome

ORPHA:2326Malform.
Autosomal recessive

Kandori fleck retina

ORPHA:99179Malform.

Kapur-Toriello syndrome

ORPHA:2328Malform.
Autosomal recessive

Karsch-Neugebauer syndrome

ORPHA:2329Malform.
Autosomal dominant