5A50.1ICD-11 MMS 2026-01
Pseudohypoparathyroidism
Description
Pseudohypoparathyroidism is a condition with refractoriness to parathyroid hormone of its target tissues especially kidney that causes hypocalcaemia and hyperphosphataemia even in the presence of high circulating levels of biologically active parathyroid hormone.
Index terms
- Pseudohypoparathyroidism
- PHP - [pseudohypoparathyroidism]
- constitutional chronic hypocalcaemia
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- familial pseudohypoparathyroidism
- parathyroid hormone resistant hypoparathyroidism
- Pseudohypoparathyroidism with Albright hereditary osteodystrophy
- AHO - [Albright hereditary osteodystrophy]
- Albright hereditary osteodystrophy, classical type
- Pseudohypoparathyroidism type 1A
- Albright hereditary osteodystrophy - pseudohypoparathyroidism type 1A
- pseudohypoparathyroidism type 1 A
- pseudohypoparathyroidism type ia
- Pseudohypoparathyroidism type 1C
- Pseudohypoparathyroidism without Albright hereditary osteodystrophy
- Pseudohypoparathyroidism type 1B
- Pseudohypoparathyroidism type 2
- Cataract in pseudohypoparathyroidism
- Pseudopseudohypoparathyroidism
- AHO - [Albright hereditary osteodystrophy] PPHP - [pseudopseudohypoparathyroidism]
- Albright hereditary osteodystrophy - pseudopseudohypoparathyroidism
Exclusions from above levels
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5C54.1– Hyperphosphataemic familial tumoural calcinosis5C63.20– Hypocalcaemic vitamin D dependent rickets5C63.21– Hypocalcaemic vitamin D resistant rickets18– Pregnancy, childbirth or the puerperium- http://id.who.int/icd/entity/1004987305 – Transitory endocrine or metabolic disorders specific to fetus or newborn
Sibling codes
Foundation entity
Pseudohypoparathyroidism – http://id.who.int/icd/entity/1225154856
Allowed postcoordination axes
Part of: 5A50: Hypoparathyroidism › 05: Endocrine, nutritional or metabolic diseases