Class information for: |
Basic class information |
| ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
|---|---|---|---|
| 24759 | 252 | 24.0 | 74% |
Classes in level above (level 2) |
| ID, lev. above |
Publications | Label for level above |
|---|---|---|
| 2292 | 4139 | MELANOCORTIN//MELANOCORTIN RECEPTOR//MELANOCORTIN RECEPTORS |
Terms with highest relevance score |
| Rank | Term | Type of term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
|---|---|---|---|---|---|---|
| 1 | TRIPLE A SYNDROME | Author keyword | 120 | 92% | 19% | 47 |
| 2 | ALACRIMA | Author keyword | 52 | 80% | 13% | 32 |
| 3 | ALLGROVE SYNDROME | Author keyword | 44 | 88% | 8% | 21 |
| 4 | AAAS GENE | Author keyword | 23 | 100% | 4% | 10 |
| 5 | FAMILIAL GLUCOCORTICOID DEFICIENCY | Author keyword | 17 | 72% | 5% | 13 |
| 6 | ALACRIMIA | Author keyword | 15 | 88% | 3% | 7 |
| 7 | ACTH RESISTANCE | Author keyword | 12 | 75% | 4% | 9 |
| 8 | GLUCOCORTICOID DEFICIENCY | Author keyword | 10 | 57% | 5% | 12 |
| 9 | AAAS GENE MUTATION | Author keyword | 8 | 100% | 2% | 5 |
| 10 | ALLGROVES SYNDROME | Author keyword | 8 | 100% | 2% | 5 |
Web of Science journal categories |
Author Key Words |
| Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
LCSH search | Wikipedia search |
|---|---|---|---|---|---|---|---|
| 1 | TRIPLE A SYNDROME | 120 | 92% | 19% | 47 | Search TRIPLE+A+SYNDROME | Search TRIPLE+A+SYNDROME |
| 2 | ALACRIMA | 52 | 80% | 13% | 32 | Search ALACRIMA | Search ALACRIMA |
| 3 | ALLGROVE SYNDROME | 44 | 88% | 8% | 21 | Search ALLGROVE+SYNDROME | Search ALLGROVE+SYNDROME |
| 4 | AAAS GENE | 23 | 100% | 4% | 10 | Search AAAS+GENE | Search AAAS+GENE |
| 5 | FAMILIAL GLUCOCORTICOID DEFICIENCY | 17 | 72% | 5% | 13 | Search FAMILIAL+GLUCOCORTICOID+DEFICIENCY | Search FAMILIAL+GLUCOCORTICOID+DEFICIENCY |
| 6 | ALACRIMIA | 15 | 88% | 3% | 7 | Search ALACRIMIA | Search ALACRIMIA |
| 7 | ACTH RESISTANCE | 12 | 75% | 4% | 9 | Search ACTH+RESISTANCE | Search ACTH+RESISTANCE |
| 8 | GLUCOCORTICOID DEFICIENCY | 10 | 57% | 5% | 12 | Search GLUCOCORTICOID+DEFICIENCY | Search GLUCOCORTICOID+DEFICIENCY |
| 9 | AAAS GENE MUTATION | 8 | 100% | 2% | 5 | Search AAAS+GENE+MUTATION | Search AAAS+GENE+MUTATION |
| 10 | ALLGROVES SYNDROME | 8 | 100% | 2% | 5 | Search ALLGROVES+SYNDROME | Search ALLGROVES+SYNDROME |
Key Words Plus |
| Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
|---|---|---|---|---|---|
| 1 | ALLGROVE SYNDROME | 103 | 93% | 15% | 39 |
| 2 | ALACRIMA | 90 | 80% | 22% | 56 |
| 3 | FAMILIAL GLUCOCORTICOID DEFICIENCY | 45 | 54% | 23% | 59 |
| 4 | AAAS GENE | 38 | 93% | 6% | 14 |
| 5 | A SYNDROME | 34 | 59% | 15% | 38 |
| 6 | TRIPLE A SYNDROME | 28 | 48% | 17% | 43 |
| 7 | SELECTIVE ACTH INSENSITIVITY | 24 | 91% | 4% | 10 |
| 8 | ACTH INSENSITIVITY | 23 | 86% | 5% | 12 |
| 9 | WD REPEAT PROTEIN | 20 | 28% | 25% | 62 |
| 10 | ADRENOCORTICOTROPIN RECEPTOR GENE | 15 | 63% | 6% | 15 |
Journals |
Reviews |
| Title | Publ. year | Cit. | Active references |
% act. ref. to same field |
|---|---|---|---|---|
| Familial glucocorticoid deficiency: New genes and mechanisms | 2013 | 7 | 26 | 54% |
| Adult or late-onset triple A syndrome Case report and literature review | 2010 | 7 | 16 | 81% |
| Inherited ACTH insensitivity illuminates the mechanisms of ACTH action | 2005 | 34 | 44 | 45% |
| Adrenocorticotropin insensitivity syndromes | 1998 | 109 | 86 | 49% |
| Familial glucocorticoid deficiency: Advances in the molecular understanding of ACTH action | 2008 | 19 | 53 | 51% |
| A novel presentation of familial glucocorticoid deficiency (FGD) and current literature review | 2004 | 9 | 28 | 89% |
| Oxidative stress and adrenocortical insufficiency | 2014 | 3 | 79 | 24% |
| The Molecular Basis of Adrenocorticotrophin Resistance Syndrome | 2009 | 1 | 89 | 66% |
| Familial glucocorticoid deficiency: One syndrome, but more than one gene | 1997 | 12 | 14 | 64% |
| The nuclear pore complex: disease associations and functional correlations | 2004 | 37 | 62 | 24% |
Address terms |
| Rank | Address term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
|---|---|---|---|---|---|
| 1 | WILLIAM HARVEY ENDOCRINOL | 2 | 67% | 0.8% | 2 |
| 2 | ENDOCRINOL MOTHER CHILD HLTH CARE | 1 | 50% | 0.4% | 1 |
| 3 | INRA INSERM U418 | 1 | 50% | 0.4% | 1 |
| 4 | INRA UA953 | 1 | 50% | 0.4% | 1 |
| 5 | PAEDIAT KANTRIDA | 1 | 50% | 0.4% | 1 |
| 6 | PEDIAT KANTRIDA | 1 | 50% | 0.4% | 1 |
| 7 | SERV CHIRURG PEDIAT B | 1 | 22% | 0.8% | 2 |
| 8 | DIGEST DIS NUTR NIH | 0 | 33% | 0.4% | 1 |
| 9 | BOALI HOSP | 0 | 25% | 0.4% | 1 |
| 10 | NEUROPED | 0 | 25% | 0.4% | 1 |
Related classes at same level (level 1) |
| Rank | Relatedness score | Related classes |
|---|---|---|
| 1 | 0.0000183912 | MELANOCORTIN//MELANOCORTIN 4 RECEPTOR//MELANOCORTIN RECEPTOR |
| 2 | 0.0000171143 | ACHALASIA//HELLER MYOTOMY//PERORAL ENDOSCOPIC MYOTOMY |
| 3 | 0.0000117047 | ADRENAL HYPOPLASIA CONGENITA//DAX 1//STEROIDOGENIC FACTOR 1 |
| 4 | 0.0000073155 | TRANSHYDROGENASE//NICOTINAMIDE NUCLEOTIDE//NICOTINAMIDE NUCLEOTIDE TRANSHYDROGENASE |
| 5 | 0.0000061340 | ALDOSTERONE BIOSYNTHESIS//ALDOSTERONE SYNTHASE DEFICIENCY//ALDOSTERONE SYNTHESIS |
| 6 | 0.0000055962 | SEPTO OPTIC DYSPLASIA//SEPTUM PELLUCIDUM//OPTIC NERVE HYPOPLASIA |
| 7 | 0.0000054686 | ACTH INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA//AIMAH//ENDOCRINE PATHOPHYSIOL |
| 8 | 0.0000053936 | STEROIDOGENIC ACUTE REGULATORY PROTEIN//STARD6//STEROIDOGENIC ACUTE REGULATORY PROTEIN STAR |
| 9 | 0.0000052154 | ADRENAL INSUFFICIENCY//RELATIVE ADRENAL INSUFFICIENCY//LOW DOSE ACTH TEST |
| 10 | 0.0000044249 | LACRIMAL GLAND//HUMAN LACRIMAL GLAND//AUTOIMMUNE DACRYOADENITIS |