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DeCS
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Descriptor English:
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Pseudohypoparathyroidism
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Descriptor Spanish:
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Seudohipoparatiroidismo
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Descriptor Portuguese:
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Pseudo-Hipoparatireoidismo
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Synonyms English:
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Albright Hereditary Osteodystrophy with Multiple Hormone Resistance
PHD Ib
PHD Ibs
PHD1b
PHP Ia
Pseudohypoparathyroidism, Type Ia
Pseudohypoparathyroidism, Type Ib
Pseudohypoparathyroidisms
Pseudohypoparathyroidisms, Type Ia
Pseudohypoparathyroidisms, Type Ib
Type Ia Pseudohypoparathyroidism
Type Ia Pseudohypoparathyroidisms
Type Ib Pseudohypoparathyroidism
Type Ib Pseudohypoparathyroidisms
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Tree Number:
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C05.116.198.709
C16.320.565.618.815
C18.452.104.709
C18.452.174.766
C18.452.648.618.815
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Definition English:
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A hereditary syndrome clinically similar to HYPOPARATHYROIDISM. It is characterized by HYPOCALCEMIA; HYPERPHOSPHATEMIA; and associated skeletal development impairment and caused by failure of response to PARATHYROID HORMONE rather than deficiencies. A severe form with resistance to multiple hormones is referred to as Type 1a and is associated with maternal mutant allele of the ALPHA CHAIN OF STIMULATORY G PROTEIN. |
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Indexing Annotation English:
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do not confuse with PSEUDOPSEUDOHYPOPARATHYROIDISM
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See Related English:
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GTP-Binding Protein alpha Subunits, Gs
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History Note English:
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65(63)
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Allowable Qualifiers English:
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Record Number:
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11984
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Unique Identifier:
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D011547
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Occurrence in VHL:
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Similar:
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DeCS
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