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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome

ORPHA:369939Malform.
Autosomal recessive

Severe myopia-generalized joint laxity-short stature syndrome

ORPHA:527450Malform.
Autosomal recessive

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

ORPHA:314655Etio. sub.
Unknown

Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency

ORPHA:397593Disease
Autosomal recessive

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

ORPHA:500545Disease
Autosomal dominant

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

ORPHA:708166Malform.
Autosomal recessive

Severe oculo-renal-cerebellar syndrome

ORPHA:2715Malform.
Autosomal recessive

Severe phosphoribosylpyrophosphate synthetase superactivity

ORPHA:411543Clin. sub.
X-linked recessive

Severe primary trimethylaminuria

ORPHA:468726Disease
Autosomal recessive

Sex cord-stromal tumor of testis

ORPHA:363489Disease

Shashi-Pena syndrome

ORPHA:689408Malform.
Autosomal dominant

Sheehan syndrome

ORPHA:91355Malform.

Sheldon-Hall syndrome

ORPHA:1147Malform.
Autosomal dominant, Not applicable

Shiga toxin-associated hemolytic uremic syndrome

ORPHA:90038Clin. sub.
Not applicable

Shigellosis

ORPHA:810Disease
Not applicable

Shone complex

ORPHA:99063Malform.

Short bowel syndrome

ORPHA:104008Clin. grp.

Short chain acyl-CoA dehydrogenase deficiency

ORPHA:26792Disease
Autosomal recessive

Short fifth metacarpals-insulin resistance syndrome

ORPHA:66518Disease
Autosomal dominant

Short rib-polydactyly syndrome

ORPHA:1505Clin. grp.
Autosomal recessive

Short rib-polydactyly syndrome type 5

ORPHA:498497Malform.
Autosomal recessive

Short rib-polydactyly syndrome, Beemer-Langer type

ORPHA:93268Malform.
Autosomal recessive

Short rib-polydactyly syndrome, Majewski type

ORPHA:93269Malform.
Autosomal recessive

Short rib-polydactyly syndrome, Saldino-Noonan type

ORPHA:93270Malform.
Autosomal recessive