MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
1,772 Erkrankungen gefunden (Malf.) Zurücksetzen

Jacobsen syndrome

ORPHA:2308Malf.
Not applicable, Unknown

Jalili syndrome

ORPHA:1873Malf.
Autosomal recessive

Jawad syndrome

ORPHA:313795Malf.
Autosomal recessive

Jeune syndrome

ORPHA:474Malf.
Autosomal recessive

Johanson-Blizzard syndrome

ORPHA:2315Malf.
Autosomal recessive

Johnson neuroectodermal syndrome

ORPHA:2316Malf.
Autosomal dominant

Joubert syndrome with Jeune asphyxiating thoracic dystrophy

ORPHA:397715Malf.
Autosomal recessive

Joubert syndrome with ocular defect

ORPHA:220493Malf.
Autosomal recessive

Joubert syndrome with oculorenal defect

ORPHA:2318Malf.
Autosomal recessive

Joubert syndrome with renal defect

ORPHA:220497Malf.
Autosomal recessive

Juberg-Hayward syndrome

ORPHA:2319Malf.
Autosomal dominant, Autosomal recessive

Jung syndrome

ORPHA:2321Malf.

Juvenile Paget disease

ORPHA:2801Malf.
Autosomal recessive

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

ORPHA:457193Malf.
Autosomal dominant

KBG syndrome

ORPHA:2332Malf.
Autosomal dominant

KDM5C-related syndromic X-linked intellectual disability

ORPHA:85279Malf.
X-linked recessive

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

ORPHA:603684Malf.
Autosomal recessive

KLHL7-related Bohring-Opitz-like syndrome

ORPHA:603689Malf.
Autosomal recessive

Kabuki syndrome

ORPHA:2322Malf.
Autosomal dominant, Not applicable

Kagami-Ogata syndrome

ORPHA:254519Malf.
Autosomal dominant, Not applicable

Kallmann syndrome-heart disease syndrome

ORPHA:2326Malf.
Autosomal recessive

Kandori fleck retina

ORPHA:99179Malf.

Kapur-Toriello syndrome

ORPHA:2328Malf.
Autosomal recessive

Karsch-Neugebauer syndrome

ORPHA:2329Malf.
Autosomal dominant