MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
3,968 diseases matched (Disease) Reset

Hypothyroidism due to deficient transcription factors involved in pituitary development or function

ORPHA:226307Disease
Autosomal dominant, Autosomal recessive

Hypotonia with lactic acidemia and hyperammonemia

ORPHA:137908Disease
Autosomal recessive

Hypotonia-cystinuria syndrome

ORPHA:163690Disease
Autosomal recessive

Hypotonia-failure to thrive-microcephaly syndrome

ORPHA:79507Disease
Autosomal recessive

Hypotonia-speech impairment-severe cognitive delay syndrome

ORPHA:371364Disease
Autosomal recessive

Hypotrichosis simplex

ORPHA:55654Disease
Autosomal dominant, Autosomal recessive

Hypotrichosis simplex of the scalp

ORPHA:90368Disease
Autosomal dominant

Hypotrichosis-deafness syndrome

ORPHA:330029Disease
Autosomal dominant

Hypotrichosis-intellectual disability, Lopes type

ORPHA:2266Disease
Autosomal recessive

Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome

ORPHA:69735Disease
Autosomal dominant, Autosomal recessive

Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome

ORPHA:307936Disease

Hypoxanthine guanine phosphoribosyltransferase partial deficiency

ORPHA:79233Disease
X-linked recessive

ICHAD syndrome

ORPHA:699599Disease
Autosomal dominant

IFIH1-related hereditary spastic paraplegia

ORPHA:689231Disease
Autosomal dominant

IL21-related infantile inflammatory bowel disease

ORPHA:477661Disease
Autosomal recessive

IRF2BPL-related regressive neurodevelopmental disorder-dystonia-seizures syndrome

ORPHA:597623Disease
Autosomal dominant

IRIDA syndrome

ORPHA:209981Disease
Autosomal recessive

IRVAN syndrome

ORPHA:209943Disease
Not applicable

ISPD-related limb-girdle muscular dystrophy R20

ORPHA:352479Disease
Autosomal recessive

ITM2B amyloidosis

ORPHA:439254Disease
Autosomal dominant

ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement

ORPHA:457375Disease
Autosomal recessive

Iatrogenic Creutzfeldt-Jakob disease

ORPHA:576379Disease

Ichthyosis follicularis-alopecia-photophobia syndrome

ORPHA:2273Disease
Autosomal dominant, Not applicable, X-linked recessive

Ichthyosis hystrix of Curth-Macklin

ORPHA:79503Disease
Autosomal dominant, Not applicable