MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
1,772 diseases matched (Malform.) Reset

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

ORPHA:94066Malform.
Autosomal recessive

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

ORPHA:391307Malform.
Autosomal recessive

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

ORPHA:324307Malform.
Unknown

Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome

ORPHA:1236Malform.
No data available

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

ORPHA:708166Malform.
Autosomal recessive

Severe oculo-renal-cerebellar syndrome

ORPHA:2715Malform.
Autosomal recessive

Shashi-Pena syndrome

ORPHA:689408Malform.
Autosomal dominant

Sheehan syndrome

ORPHA:91355Malform.

Sheldon-Hall syndrome

ORPHA:1147Malform.
Autosomal dominant, Not applicable

Shone complex

ORPHA:99063Malform.

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

Short rib-polydactyly syndrome, Verma-Naumoff type

ORPHA:93271Malform.
Autosomal recessive

Short stature, Brussels type

ORPHA:2867Malform.
Unknown

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

ORPHA:397623Malform.
Autosomal recessive

Short stature-brachydactyly-obesity-global developmental delay syndrome

ORPHA:464288Malform.
Autosomal recessive

Short stature-craniofacial anomalies-genital hypoplasia syndrome

ORPHA:2994Malform.

Short stature-deafness-neutrophil dysfunction-dysmorphism syndrome

ORPHA:2866Malform.

Short stature-optic atrophy-Pelger-Huët anomaly syndrome

ORPHA:391677Malform.
Autosomal recessive

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

ORPHA:589442Malform.
Autosomal recessive