# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.disease_name
Pulmonary arterial hypertension associated with congenital heart disease

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.icd10_category
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.icd10_category
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.icd10_category
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.disease_name
Autosomal dominant polycystic kidney disease

# data[].attributes.icd10_category
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.disease_name
Generalized epilepsy with febrile seizures-plus

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.icd10_category
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.disease_name
Glycogen storage disease due to muscle glycogen phosphorylase deficiency

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.disease_name
Rare congenital non-syndromic heart malformation

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.disease_name
Ocular albinism with congenital sensorineural deafness

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.disease_name
Facial onset sensory and motor neuronopathy

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.disease_name
NON RARE IN EUROPE: Heterozygous familial hypercholesterolemia

# data[].attributes.icd10_category
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

# data[].attributes.icd10_category
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

# data[].attributes.icd10_category
Diseases of the skin and subcutaneous tissue

# data[].attributes.icd10_category
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

# data[].attributes.icd10_category
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.icd10_category
Diseases of the musculoskeletal system and connective tissue

# data[].attributes.icd10_category
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

# data[].attributes.icd10_category
Diseases of the musculoskeletal system and connective tissue

# data[].attributes.icd10_category
Diseases of the musculoskeletal system and connective tissue

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.disease_name
Autosomal recessive polycystic kidney disease

# data[].attributes.disease_name
Torsade-de-pointes syndrome with short coupling interval

# data[].attributes.disease_name
Overgrowth or tall stature syndrome with skeletal involvement

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.disease_name
Short chain acyl-CoA dehydrogenase deficiency

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.disease_name
NON RARE IN EUROPE: Familial isolated hypertrophic cardiomyopathy

# data[].attributes.disease_name
Hypogonadotropic hypogonadism with Fertile Eunuch phenotype

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.disease_name
Hypogonadotropic hypogonadism with partial puberty phenotype

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.disease_name
Hypogonadotropic hypogonadism with absent puberty phenotype

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.disease_name
NON RARE IN EUROPE: Hyperlipoproteinemia type 4

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

# data[].attributes.disease_name
Syndrome with 46,XY disorder of sex development

# data[].attributes.icd10_category
Endocrine, nutritional and metabolic diseases

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