Visão selecionada em Inglês
| Descritor em português: | Pseudo-Hipoparatireoidismo | ||||||
| Descritor em inglês: | Pseudohypoparathyroidism | ||||||
| Descritor em espanhol: |
Seudohipoparatiroidismo
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| Descritor em francês: | Pseudohypoparathyroïdie | ||||||
| Termo(s) alternativo(s): |
Albright Hereditary Osteodystrophy Albright Hereditary Osteodystrophy with Multiple Hormone Resistance Hereditary Osteodystrophy, Albright Osteodystrophy, Albright Hereditary PHD Ib PHD Ibs PHD1b PHP Ia PHPIa 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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| Código(s) hierárquico(s): |
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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| Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D011547 | ||||||
| Nota de escopo: | 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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| Nota de indexação: | do not confuse with PSEUDOPSEUDOHYPOPARATHYROIDISM |
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| Qualificadores permitidos: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Nota MeSH pública: | 65 |
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| Nota histórica: | 65(63) |
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| Veja também os descritores: |
GTP-Binding Protein alpha Subunits, Gs
MeSH | ||||||
| Identificador DeCS: | 11984 | ||||||
| ID do descritor: | D011547 | ||||||
| Documentos indexados na Biblioteca Virtual em Saúde (BVS): | Clique aqui para acessar os documentos da BVS | ||||||
| Data de estabelecimento: | 01/01/1965 | ||||||
| Data de entrada: | 01/01/1999 | ||||||
| Data de revisão: | 27/05/2020 |
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Pseudohypoparathyroidism
- Conceito preferido
Pseudohypoparathyroidism, Type Ib
- Mais específico
Pseudohypoparathyroidism, Type Ia
- Mais específico
| Identificador do conceito |
M0017949 |
| Nota de escopo | 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. |
| Termo preferido | Pseudohypoparathyroidism |
| Termo(s) alternativo(s) |
Pseudohypoparathyroidisms |
| Identificador do conceito |
M0566696 |
| Termo preferido | Pseudohypoparathyroidism, Type Ib |
| Termo(s) alternativo(s) |
PHD Ib PHD Ibs PHD1b Pseudohypoparathyroidisms, Type Ib Type Ib Pseudohypoparathyroidism Type Ib Pseudohypoparathyroidisms |
| Identificador do conceito |
M0570744 |
| Nota de escopo | A syndrome characterized by variable features such as short stature, obesity, round face, subcutaneous ossifications, and BRACHYDACTYLY. It is associated with resistance to PARATHYROID HORMONE and THYROTROPIN. The autosomal dominant inherited form (PSEUDOHYPOPARATHYROIDISM, TYPE IA) is caused by mutations in the GNAS gene. OMIM: 103580. |
| Termo preferido | Pseudohypoparathyroidism, Type Ia |
| Termo(s) alternativo(s) |
Albright Hereditary Osteodystrophy Albright Hereditary Osteodystrophy with Multiple Hormone Resistance Hereditary Osteodystrophy, Albright Osteodystrophy, Albright Hereditary PHP Ia PHPIa Pseudohypoparathyroidisms, Type Ia Type Ia Pseudohypoparathyroidism Type Ia Pseudohypoparathyroidisms |
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