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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Albright's hereditary osteodystrophy  
pseudohypoparathyroidism type IB  
Pseudohypoparathyroidism Type IC  
Pseudohypoparathyroidism Type II 
pseudopseudohypoparathyroidism  
A form of PSEUDOHYPOPARATHYROIDISM characterized by the same features except for the abnormal response to hormones such as PARATHYROID HORMONE. It is associated with paternally inherited mutant alleles of the ALPHA CHAIN OF STIMULATORY G PROTEIN.

Synonyms
Exact Synonyms: Albright Hereditary Osteodystrophy without Multiple Hormone Resistance ;   PPHP ;   Pseudo-Pseudohypoparathyroidisms ;   Pseudopseudo Hypoparathyroidism ;   Pseudopseudo-Hypoparathyroidisms ;   normocalcemic pseudohypoparathyroidism ;   pseudo pseudohypoparathyroidism ;   pseudopseudohypoparathyroidisms
Primary IDs: MESH:D011556
Alternate IDs: OMIM:612463
Xrefs: GARD:7860 ;   NCI:C129722
Definition Sources: MESH:D011556

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