| Descriptor English: | Hypoadrenocorticism, Familial | ||||||
| Descriptor Spanish: |
Insuficiencia Corticosuprarrenal Familiar
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| Descriptor Portuguese: | Hipoadrenocorticismo Familiar | ||||||
| Descriptor French: | Maladie d'Addison familiale | ||||||
| Entry term(s): |
AHC with Isolated Gonadotropin Deficiency Addison Disease, X Linked Addison Disease, X-Linked Adrenal Hypoplasia, Congenital Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism Adrenal Hypoplasia, X-linked Complex Glycerol Kinase Deficiency Congenital Adrenal Hypoplasia Congenital Adrenal Hypoplasias Cytomegalic Adrenocortical Hypoplasia Cytomegalic Adrenocortical Hypoplasias Familial Hypoadrenocorticism Familial Hypoadrenocorticisms Familial X linked Addison Disease Familial X-linked Addison Disease Hypoadrenocorticisms, Familial Hypoplasia, Congenital Adrenal X linked Adrenal Hypoplasia X linked Congenital Adrenal Hypoplasia X-Linked Addison Disease X-linked Adrenal Hypoplasia X-linked Congenital Adrenal Hypoplasia Xp21 Contiguous Gene Deletion Syndrome |
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| Tree number(s): |
C19.053.500.263.500 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D000075262 | ||||||
| Scope note: | Hereditary forms of Addison disease that may exhibit autosomal recessive or X-linked inheritance. They are characterized by severe neurological symptoms, APNEA; and death in infancy. OMIM: 240200 |
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| Allowable Qualifiers: |
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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| Public MeSH Note: | 2018; HYPOADRENOCORTICISM, FAMILIAL was indexed under ADRENAL INSUFFICIENCY 2010-2017 |
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| History Note: | 2018(2010) |
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| DeCS ID: | 56957 | ||||||
| Unique ID: | D000075262 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2018/01/01 | ||||||
| Date of Entry: | 2017/07/11 | ||||||
| Revision Date: | 2017/06/20 |
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Hypoadrenocorticism, Familial
- Preferred
Complex Glycerol Kinase Deficiency
- Narrower
Xp21 Contiguous Gene Deletion Syndrome
- Broader
X-linked Adrenal Hypoplasia
- Narrower
| Concept UI |
M000630038 |
| Scope note | Hereditary forms of Addison disease that may exhibit autosomal recessive or X-linked inheritance. They are characterized by severe neurological symptoms, APNEA; and death in infancy. OMIM: 240200 |
| Preferred term | Hypoadrenocorticism, Familial |
| Entry term(s) |
Familial Hypoadrenocorticism Familial Hypoadrenocorticisms Hypoadrenocorticisms, Familial |
| Concept UI |
M000630039 |
| Preferred term | Complex Glycerol Kinase Deficiency |
| Concept UI |
M000630042 |
| Preferred term | Xp21 Contiguous Gene Deletion Syndrome |
| Concept UI |
M000630037 |
| Preferred term | X-linked Adrenal Hypoplasia |
| Entry term(s) |
AHC with Isolated Gonadotropin Deficiency Addison Disease, X Linked Addison Disease, X-Linked Adrenal Hypoplasia, Congenital Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism Adrenal Hypoplasia, X-linked Congenital Adrenal Hypoplasia Congenital Adrenal Hypoplasias Cytomegalic Adrenocortical Hypoplasia Cytomegalic Adrenocortical Hypoplasias Familial X linked Addison Disease Familial X-linked Addison Disease Hypoplasia, Congenital Adrenal X linked Adrenal Hypoplasia X linked Congenital Adrenal Hypoplasia X-Linked Addison Disease X-linked Congenital Adrenal Hypoplasia |
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