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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:369939Порок
Autosomal recessive

Severe myopia-generalized joint laxity-short stature syndrome

ORPHA:527450Порок
Autosomal recessive

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

ORPHA:314655Этиол. подт.
Unknown

Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency

ORPHA:397593Заболевание
Autosomal recessive

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

ORPHA:500545Заболевание
Autosomal dominant

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

ORPHA:708166Порок
Autosomal recessive

Severe oculo-renal-cerebellar syndrome

ORPHA:2715Порок
Autosomal recessive

Severe phosphoribosylpyrophosphate synthetase superactivity

ORPHA:411543Клин. подт.
X-linked recessive

Severe primary trimethylaminuria

ORPHA:468726Заболевание
Autosomal recessive

Sex cord-stromal tumor of testis

ORPHA:363489Заболевание

Shashi-Pena syndrome

ORPHA:689408Порок
Autosomal dominant

Sheehan syndrome

ORPHA:91355Порок

Sheldon-Hall syndrome

ORPHA:1147Порок
Autosomal dominant, Not applicable

Shiga toxin-associated hemolytic uremic syndrome

ORPHA:90038Клин. подт.
Not applicable

Shigellosis

ORPHA:810Заболевание
Not applicable

Shone complex

ORPHA:99063Порок

Short bowel syndrome

ORPHA:104008Клин. гр.

Short chain acyl-CoA dehydrogenase deficiency

ORPHA:26792Заболевание
Autosomal recessive

Short fifth metacarpals-insulin resistance syndrome

ORPHA:66518Заболевание
Autosomal dominant

Short rib-polydactyly syndrome

ORPHA:1505Клин. гр.
Autosomal recessive

Short rib-polydactyly syndrome type 5

ORPHA:498497Порок
Autosomal recessive

Short rib-polydactyly syndrome, Beemer-Langer type

ORPHA:93268Порок
Autosomal recessive

Short rib-polydactyly syndrome, Majewski type

ORPHA:93269Порок
Autosomal recessive

Short rib-polydactyly syndrome, Saldino-Noonan type

ORPHA:93270Порок
Autosomal recessive