Trusted information across 10,888 rare diseases — plain language, always cited, free for everyone.
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Showing 8,901-8,920 of 10,888 diseases
MONDO:0014227
MONDO:0009009
Hypoplasminogenemia is a rare multisystem condition marked by markedly impaired extracellular fibrinolysis, leading to the development of ligneous pse...
MONDO:0004933
Hypoplastic left heart syndrome (HLHS) is a congenital heart condition characterized by the underdevelopment of left-sided cardiac structures, includi...
MONDO:0009433
Hypoplastic left heart syndrome 1 is a congenital heart defect that primarily affects the structures on the left side of the heart. It involves underd...
MONDO:0013752
Hypoplastic left heart syndrome 2 is a congenital heart condition characterized by underdevelopment of the left-sided heart structures. This variant i...
MONDO:0017400
MONDO:0020291
Hypoplastic right heart syndrome is a rare congenital heart condition characterized by the underdevelopment of the right-sided heart structures, inclu...
MONDO:0009434
Hypoproteinemia, hypercatabolic (also called Beta-2-microglobulin deficiency or immunodeficiency 43) is an inherited disorder that primarily affects t...
MONDO:0001036
MONDO:0001035
MONDO:0010384
Hypospadias 1, X-linked is a congenital condition primarily affecting male infants and involves an abnormal placement of the urethral opening on the p...
MONDO:0010423
Hypospadias 2, X-linked is a congenital condition that primarily affects the development of the male external genitalia, where the urethral opening is...
MONDO:0007802
Hypospadias 3, autosomal is a congenital condition that primarily affects the development of the male genitalia, resulting in an abnormally placed ure...
MONDO:0010458
Hypospadias 4, X-linked is a congenital condition primarily affecting the development of the male urogenital system, where the urethral opening is abn...
MONDO:0009435
MONDO:0018620
MONDO:0019484
Hypothalamic hamartomas with gelastic seizures is a rare cerebral malformation characterized by a developmental abnormality in the hypothalamus that l...
MONDO:0010142
Hypothyroidism due to TSH receptor mutations is a form of primary congenital hypothyroidism in which the thyroid gland is resistant to the actions of...
MONDO:0016411
Hypothyroidism due to deficient transcription factors involved in pituitary development or function is a form of central congenital hypothyroidism tha...
MONDO:0043103
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