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

NEK9-related lethal skeletal dysplasia

ORPHA:464366Malf.
Autosomal recessive

NKAP-related intellectual disability-facial dysmorphism-marfanoid habitus-scoliosis syndrome

ORPHA:700325Malf.
X-linked recessive

NPHP3-related Meckel-like syndrome

ORPHA:3032Malf.
Autosomal recessive

NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance

ORPHA:600663Malf.
Autosomal recessive

Nager syndrome

ORPHA:245Malf.
Autosomal dominant, Autosomal recessive, Not applicable

Nail-patella syndrome

ORPHA:2614Malf.
Autosomal dominant

Nance-Horan syndrome

ORPHA:627Malf.
X-linked dominant

Nanophthalmos

ORPHA:35612Malf.
Autosomal dominant, Autosomal recessive, Not applicable

Nasopalpebral lipoma-coloboma syndrome

ORPHA:2399Malf.
Autosomal dominant

Nasu-Hakola disease

ORPHA:2770Malf.
Autosomal recessive

Nathalie syndrome

ORPHA:2663Malf.

Native American myopathy

ORPHA:168572Malf.
Autosomal recessive

Nephropathy-deafness-hyperparathyroidism syndrome

ORPHA:2668Malf.
Autosomal recessive

Nephrosis-deafness-urinary tract-digital malformations syndrome

ORPHA:2669Malf.
Unknown

Nestor-Guillermo progeria syndrome

ORPHA:280576Malf.
Autosomal recessive

Neu-Laxova syndrome

ORPHA:2671Malf.
Autosomal recessive

Neuhauser-Eichner-Opitz syndrome

ORPHA:2672Malf.
Autosomal dominant

Neurodevelopmental delay-brain malformations-skeletal defects-intellectual disability syndrome

ORPHA:662207Malf.
Autosomal dominant

Neurodevelopmental delay-congenital heart defects-intellectual disability syndrome

ORPHA:662234Malf.
Autosomal dominant

Neurodevelopmental delay-intellectual disability-skeletal defects syndrome

ORPHA:662198Malf.
X-linked dominant

Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome

ORPHA:529665Malf.
Autosomal recessive

Neurodevelopmental disorder-brain malformation-facial dysmorphism-brachydactyly syndrome

ORPHA:662189Malf.
Autosomal dominant

Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome

ORPHA:453499Malf.
Autosomal dominant, Not applicable

Neurodevelopmental disorder-slit-like lateral ventricles-intellectual disability syndrome

ORPHA:664430Malf.
Autosomal recessive