| Descriptor English: | Focal Dermal Hypoplasia | ||||||
| Descriptor Spanish: |
Hipoplasia Dérmica Focal
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| Descriptor Portuguese: | Hipoplasia Dérmica Focal | ||||||
| Descriptor French: | Hypoplasie dermique en aires | ||||||
| Entry term(s): |
Dermal Hypoplasia, Focal Dermal Hypoplasias, Focal Focal Dermal Hypoplasias Goltz Gorlin Syndrome Goltz Syndrome Goltz's Syndrome Goltz-Gorlin Syndrome Goltzs Syndrome Gorlin Syndrome, Goltz Hypoplasia, Focal Dermal Hypoplasias, Focal Dermal Syndrome, Goltz Syndrome, Goltz Gorlin Syndrome, Goltz's Syndrome, Goltz-Gorlin |
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| Tree number(s): |
C05.116.099.370.380 C16.131.077.350.424 C16.131.831.350.424 C16.320.322.186 C16.320.850.250.424 C17.800.804.350.424 C17.800.827.250.424 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D005489 | ||||||
| Scope note: | A genetic skin disease characterized by hypoplasia of the dermis, herniations of fat, and hand anomalies. It is found exclusively in females and transmitted as an X-linked dominant trait. |
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| Annotation: | do not confuse entry term GOLTZ-GORLIN SYNDROME with GORLIN-GOLTZ SYNDROME see BASAL CELL NEVUS SYNDROME |
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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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| Previous Indexing: |
Abnormalities, Multiple (1968-1984) Skin (1966-1984) Skin Diseases (1966-1984) |
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| Public MeSH Note: | 91; was see under ECTODERMAL DYSPLASIA 1987-90, was see under ECTODERMAL DEFECT, CONGENITAL 1985-86; GOLTZ-GORLIN SYNDROME was see FOCAL DERMAL HYPOPLASIA 1985-92 |
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| Online Note: | use FOCAL DERMAL HYPOPLASIA to search GOLTZ-GORLIN SYNDROME 1985-92 |
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| History Note: | 91(85); was see under ECTODERMAL DYSPLASIA 1987-90, was see under ECTODERMAL DEFECT, CONGENITAL 1985-86; GOLTZ-GORLIN SYNDROME was see FOCAL DERMAL HYPOPLASIA 1985-92 |
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| DeCS ID: | 22468 | ||||||
| Unique ID: | D005489 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1991/01/01 | ||||||
| Date of Entry: | 1984/04/05 | ||||||
| Revision Date: | 2015/06/18 |
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Focal Dermal Hypoplasia
- Preferred
| Concept UI |
M0008655 |
| Scope note | A genetic skin disease characterized by hypoplasia of the dermis, herniations of fat, and hand anomalies. It is found exclusively in females and transmitted as an X-linked dominant trait. |
| Preferred term | Focal Dermal Hypoplasia |
| Entry term(s) |
Dermal Hypoplasia, Focal Dermal Hypoplasias, Focal Focal Dermal Hypoplasias Goltz Gorlin Syndrome Goltz Syndrome Goltz's Syndrome Goltz-Gorlin Syndrome Goltzs Syndrome Gorlin Syndrome, Goltz Hypoplasia, Focal Dermal Hypoplasias, Focal Dermal Syndrome, Goltz Syndrome, Goltz Gorlin Syndrome, Goltz's Syndrome, Goltz-Gorlin |
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