| D007223 |
Infant |
A child between 1 and 23 months of age. |
Infants |
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| D008297 |
Male |
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Males |
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| D011547 |
Pseudohypoparathyroidism |
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. |
Albright Hereditary Osteodystrophy,PHPIa,Albright Hereditary Osteodystrophy with Multiple Hormone Resistance,PHD Ib,PHD1b,PHP Ia,Pseudohypoparathyroidism Type 1B,Pseudohypoparathyroidism, Type Ia,Pseudohypoparathyroidism, Type Ib,Hereditary Osteodystrophy, Albright,Osteodystrophy, Albright Hereditary,Pseudohypoparathyroidism Type 1Bs,Pseudohypoparathyroidisms,Pseudohypoparathyroidisms, Type Ia,Pseudohypoparathyroidisms, Type Ib,Type Ia Pseudohypoparathyroidism,Type Ia Pseudohypoparathyroidisms,Type Ib Pseudohypoparathyroidism,Type Ib Pseudohypoparathyroidisms |
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| D002864 |
Chromogranins |
A group of acidic proteins that are major components of SECRETORY GRANULES in the endocrine and neuroendocrine cells. They play important roles in the aggregation, packaging, sorting, and processing of secretory protein prior to secretion. They are cleaved to release biologically active peptides. There are various types of granins, usually classified by their sources. |
Chromogranin,Granin,Secretogranin,Secretogranins,Granins |
|
| D003409 |
Congenital Hypothyroidism |
A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA. |
Cretinism,Myxedema, Congenital,Endemic Cretinism,Fetal Iodine Deficiency Disorder,Cretinism, Endemic,Hypothyroidism, Congenital |
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| D003951 |
Diagnostic Errors |
Incorrect or incomplete diagnoses following clinical or technical diagnostic procedures. |
Diagnostic Blind Spots,Errors, Diagnostic,Misdiagnosis,Blind Spot, Diagnostic,Blind Spots, Diagnostic,Diagnostic Blind Spot,Diagnostic Error,Error, Diagnostic,Misdiagnoses |
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| D006801 |
Humans |
Members of the species Homo sapiens. |
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man |
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| D019205 |
GTP-Binding Protein alpha Subunits, Gs |
A family of heterotrimeric GTP-binding protein alpha subunits that activate ADENYLYL CYCLASES. |
G-Protein, Gs alpha Family,G-Protein, Stimulatory Gs,G(s), alpha Subunit,G(s)alpha,Gs Stimulatory G-Proteins,Gs alpha GTP-Binding Protein Subunits,Gs, Stimulatory G-Protein,Ns Protein, Regulatory,Stimulatory GTP-Binding Protein, alpha Subunit,alpha-Gs,G Protein, Gs alpha Family,G Protein, Stimulatory Gs,G-Protein Gs, Stimulatory,G-Proteins, Gs Stimulatory,GTP Binding Protein alpha Subunits, Gs,Gs G-Protein, Stimulatory,Gs Stimulatory G Proteins,Gs alpha GTP Binding Protein Subunits,Gs, Stimulatory G Protein,Regulatory Ns Protein,Stimulatory G-Protein Gs,Stimulatory G-Proteins, Gs,Stimulatory GTP Binding Protein, alpha Subunit,Stimulatory Gs G-Protein,alpha Gs |
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