Lista chorób rzadkich*

95505 - Pituitary hormone deficiency of meningeal origin

95506 - Primary hypophysitis

95507 - Congenital anomaly of hepatic vein

95510 - Atrial appendage anomaly

95512 - Adenohypophysitis

95513 - Panhypophysitis

95611 - Pituitary hormone deficiency of vascular origin

95613 - Pituitary apoplexy

95614 - OBSOLETE: Pituitary deficiency secondary to meningeal hemorrhage

95615 - OBSOLETE: Pituitary deficiency secondary to an anevrysm

95617 - Pituitary hormone deficiency secondary to a granulomatous disease

95618 - Pituitary hormone deficiency secondary to storage disease

95619 - Post-traumatic pituitary deficiency

95621 - OBSOLETE: Postsurgical hypopituitarism

95622 - OBSOLETE: Radiation-induced hypopituitarism

95623 - OBSOLETE: Posttraumatic hypopituitarism

95625 - OBSOLETE: Posttraumatic diabetes insipidus

95626 - Acquired central diabetes insipidus

95698 - NON RARE IN EUROPE: Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency

95699 - Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency

95700 - Familial adrenal hypoplasia with absent pituitary luteinizing hormone

95701 - OBSOLETE: Congenital adrenal hypoplasia of maternal cause

95702 - X-linked adrenal hypoplasia congenita

95706 - Non-syndromic posterior hypospadias

95707 - Idiopathic isolated micropenis

95708 - Rare precocious puberty

95709 - Acquired premature ovarian failure

95710 - Non-acquired premature ovarian failure

95711 - Congenital hypothyroidism due to developmental anomaly

95712 - Thyroid ectopia

95713 - Athyreosis

95714 - Primary congenital hypothyroidism without thyroid developmental anomaly

95715 - Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies

95716 - Familial thyroid dyshormonogenesis

95717 - Idiopathic congenital hypothyroidism

95718 - Congenital thyroid malformation without hypothyroidism

95719 - Thyroid hemiagenesis

95720 - Thyroid hypoplasia

95721 - OBSOLETE: Thyroid pyramidal lobe

95854 - Levocardia

96055 - Tetrasomy 21

96059 - Mosaic trisomy 4

96060 - Mosaic trisomy 5

96061 - Mosaic trisomy 8

96063 - Mosaic trisomy 10

96068 - Mosaic trisomy 22

96069 - Distal trisomy 1p36

96070 - Distal trisomy 2p

96071 - Distal trisomy 3p

96072 - 4p16.3 microduplication syndrome

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