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

Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia

ORPHA:94066Malf.
Autosomal recessive

Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome

ORPHA:391307Malf.
Autosomal recessive

Severe lateral tibial bowing-short stature-mild winged scapula-mild facial dysmorphism syndrome

ORPHA:324307Malf.
Unknown

Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome

ORPHA:1236Malf.
No data available

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

ORPHA:708166Malf.
Autosomal recessive

Severe oculo-renal-cerebellar syndrome

ORPHA:2715Malf.
Autosomal recessive

Shashi-Pena syndrome

ORPHA:689408Malf.
Autosomal dominant

Sheehan syndrome

ORPHA:91355Malf.

Sheldon-Hall syndrome

ORPHA:1147Malf.
Autosomal dominant, Not applicable

Shone complex

ORPHA:99063Malf.

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

Short rib-polydactyly syndrome, Verma-Naumoff type

ORPHA:93271Malf.
Autosomal recessive

Short stature, Brussels type

ORPHA:2867Malf.
Unknown

Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome

ORPHA:397623Malf.
Autosomal recessive

Short stature-brachydactyly-obesity-global developmental delay syndrome

ORPHA:464288Malf.
Autosomal recessive

Short stature-craniofacial anomalies-genital hypoplasia syndrome

ORPHA:2994Malf.

Short stature-deafness-neutrophil dysfunction-dysmorphism syndrome

ORPHA:2866Malf.

Short stature-optic atrophy-Pelger-Huët anomaly syndrome

ORPHA:391677Malf.
Autosomal recessive

Short stature-skeletal dysplasia-retinal degeneration-intellectual disability-sensorineural hearing loss syndrome

ORPHA:589442Malf.
Autosomal recessive