MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome

ORPHA:369939Malf.
Autosomal recessive

Severe myopia-generalized joint laxity-short stature syndrome

ORPHA:527450Malf.
Autosomal recessive

Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion

ORPHA:314655Ätl. subt.
Unknown

Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency

ORPHA:397593Kr.
Autosomal recessive

Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract

ORPHA:500545Kr.
Autosomal dominant

Severe neurodevelopmental disorder-facial dysmorphism-cerebral-renal-cardiac anomalies syndrome

ORPHA:708166Malf.
Autosomal recessive

Severe oculo-renal-cerebellar syndrome

ORPHA:2715Malf.
Autosomal recessive

Severe phosphoribosylpyrophosphate synthetase superactivity

ORPHA:411543Kl. subt.
X-linked recessive

Severe primary trimethylaminuria

ORPHA:468726Kr.
Autosomal recessive

Sex cord-stromal tumor of testis

ORPHA:363489Kr.

Shashi-Pena syndrome

ORPHA:689408Malf.
Autosomal dominant

Sheehan syndrome

ORPHA:91355Malf.

Sheldon-Hall syndrome

ORPHA:1147Malf.
Autosomal dominant, Not applicable

Shiga toxin-associated hemolytic uremic syndrome

ORPHA:90038Kl. subt.
Not applicable

Shigellosis

ORPHA:810Kr.
Not applicable

Shone complex

ORPHA:99063Malf.

Short bowel syndrome

ORPHA:104008Kl. gruppe

Short chain acyl-CoA dehydrogenase deficiency

ORPHA:26792Kr.
Autosomal recessive

Short fifth metacarpals-insulin resistance syndrome

ORPHA:66518Kr.
Autosomal dominant

Short rib-polydactyly syndrome

ORPHA:1505Kl. gruppe
Autosomal recessive

Short rib-polydactyly syndrome type 5

ORPHA:498497Malf.
Autosomal recessive

Short rib-polydactyly syndrome, Beemer-Langer type

ORPHA:93268Malf.
Autosomal recessive

Short rib-polydactyly syndrome, Majewski type

ORPHA:93269Malf.
Autosomal recessive

Short rib-polydactyly syndrome, Saldino-Noonan type

ORPHA:93270Malf.
Autosomal recessive