Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

8 matching diseasesClear search ×

TSH-secreting pituitary adenoma

Pituitary thyrotrophic adenoma · TSH-oma

ORPHA:91347

Familial hyperthyroidism due to mutations in TSH receptor

Familial non-immune hyperthyroidism · Resistance to thyroid stimulating hormone

ORPHA:424

Functioning pituitary adenoma

Endocrine active pituitary adenoma · Secreting pituitary adenoma

ORPHA:314753

Isolated thyroid-stimulating hormone deficiency

Isolated thyrotropin deficiency · Isolated TSH deficiency

ORPHA:90674

Mixed functioning pituitary adenoma

Mixed secreting pituitary adenoma

ORPHA:314759

Pituitary resistance to thyroid hormone

PRTH · Selective pituitary resistance to thyroid hormone

ORPHA:165994

Prolactinoma

Lactotroph adenoma · PRL-secreting pituitary adenoma

ORPHA:2965

Somatomammotropinoma

Somatoprolactinoma · Somatolactotropinoma

ORPHA:314769