Rare (orphan) diseases
The full catalogue of 7,547 diseases with genetics, phenotypes, epidemiology, orphan drugs, and clinical trials.
Hypothyroidism due to deficient transcription factors involved in pituitary development or function
Autosomal dominant, Autosomal recessive
Infancy
Hypotonia with lactic acidemia and hyperammonemia
Autosomal recessive
Antenatal, Neonatal
Hypotonia-cystinuria syndrome
Autosomal recessive
Infancy, Neonatal
Hypotonia-failure to thrive-microcephaly syndrome
Autosomal recessive
Infancy, Neonatal
Hypotonia-speech impairment-severe cognitive delay syndrome
Autosomal recessive
Infancy, Neonatal
Hypotrichosis simplex
Autosomal dominant, Autosomal recessive
Childhood
Hypotrichosis simplex of the scalp
Autosomal dominant
Childhood
Hypotrichosis-deafness syndrome
Autosomal dominant
Infancy, Neonatal
Hypotrichosis-intellectual disability, Lopes type
Autosomal recessive
Childhood, Infancy
Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome
Infancy, Neonatal
Hypoxanthine guanine phosphoribosyltransferase partial deficiency
X-linked recessive
All ages
ICHAD syndrome
Autosomal dominant
IFIH1-related hereditary spastic paraplegia
Autosomal dominant
IL21-related infantile inflammatory bowel disease
Autosomal recessive
Infancy
IRF2BPL-related regressive neurodevelopmental disorder-dystonia-seizures syndrome
Autosomal dominant
Childhood, Infancy, Neonatal
IRIDA syndrome
Autosomal recessive
Infancy, Neonatal
IRVAN syndrome
Not applicable
Adolescent, Adult, Childhood
ISPD-related limb-girdle muscular dystrophy R20
Autosomal recessive
Childhood, Infancy
ITM2B amyloidosis
Autosomal dominant
Adult
ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement
Autosomal recessive
Infancy, Neonatal
Iatrogenic Creutzfeldt-Jakob disease
Adult
Ichthyosis follicularis-alopecia-photophobia syndrome
Autosomal dominant, Not applicable, X-linked recessive
Infancy, Neonatal
Ichthyosis hystrix of Curth-Macklin
Autosomal dominant, Not applicable
Childhood