| Descriptor English: | Hallermann's Syndrome | ||||||
| Descriptor Spanish: |
Síndrome de Hallermann
| ||||||
| Descriptor Portuguese: | Síndrome de Hallermann | ||||||
| Descriptor French: | Syndrome d'Hallermann-Streiff-François | ||||||
| Entry term(s): |
Dyscephalic Syndrome, Francois Dyscephalic Syndromes, Francois Francois Dyscephalic Syndrome Francois Dyscephalic Syndromes Hallermann Streiff Francois Syndrome Hallermann Streiff Syndrome Hallermann Syndrome Hallermann-Streiff Syndrome Hallermanns Syndrome Syndrome, Francois Dyscephalic Syndrome, Hallermann's Syndrome, Hallermann-Streiff Syndromes, Francois Dyscephalic |
||||||
| Tree number(s): |
C05.116.099.370.231.427 C05.660.207.231.427 C16.131.621.207.231.427 |
||||||
| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D006210 | ||||||
| Scope note: | An oculomandibulofacial syndrome principally characterized by dyscephaly (usually brachycephaly), parrot nose, mandibular hypoplasia, proportionate nanism, hypotrichosis, bilateral congenital cataracts, and microphthalmia. (Dorland, 27th ed) |
||||||
| Annotation: | a form of craniofacial dysostosis with other abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES |
||||||
| 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 |
||||||
| Public MeSH Note: | 91; was see under CRANIOFACIAL DYSOSTOSIS 1985-90; was see under MANDIBULOFACIAL DYSOSTOSIS 1965-84 |
||||||
| History Note: | 91(65); was see under CRANIOFACIAL DYSOSTOSIS 1985-90; was see under MANDIBULOFACIAL DYSOSTOSIS 1965-84 |
||||||
| DeCS ID: | 6363 | ||||||
| Unique ID: | D006210 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1991/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2012/07/03 |
|
|
Hallermann's Syndrome
- Preferred
| Concept UI |
M0009760 |
| Scope note | An oculomandibulofacial syndrome principally characterized by dyscephaly (usually brachycephaly), parrot nose, mandibular hypoplasia, proportionate nanism, hypotrichosis, bilateral congenital cataracts, and microphthalmia. (Dorland, 27th ed) |
| Preferred term | Hallermann's Syndrome |
| Entry term(s) |
Dyscephalic Syndrome, Francois Dyscephalic Syndromes, Francois Francois Dyscephalic Syndrome Francois Dyscephalic Syndromes Hallermann Streiff Francois Syndrome Hallermann Streiff Syndrome Hallermann Syndrome Hallermann-Streiff Syndrome Hallermanns Syndrome Syndrome, Francois Dyscephalic Syndrome, Hallermann's Syndrome, Hallermann-Streiff Syndromes, Francois Dyscephalic |
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey
