MeSH Browser

MeSH Heading: Facial Hemiatrophy
Tree Number(s): C07.465.284; C07.465.299.375; C10.292.319.375
Unique ID: D005150
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D005150
Annotation: do not confuse with FACIAL ASYMMETRY; note HEMIFACIAL MICROSOMIA see FACIAL ASYMMETRY
Scope Note: A syndrome characterized by slowly progressive unilateral atrophy of facial subcutaneous fat, muscle tissue, skin, cartilage, and bone. The condition typically progresses over a period of 2-10 years and then stabilizes.
Entry Term(s): Facial Hemiatrophy of Romberg; Hemifacial Atrophy; Hemifacial Atrophy, Progressive; Parry-Romberg Disease; Parry-Romberg Syndrome; Progressive Facial Hemiatrophy; Progressive Hemifacial Atrophy; Romberg Disease; Romberg Hemi-Facial Atrophy; Romberg's Disease
Public MeSH Note: for ROMBERG DISEASE see ROMBERG'S DISEASE 1963-97
Date Established: 1966/01/01
Date of Entry: 1999/01/01
Revision Date: 2015/06/22

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

congenital (CN)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Stomatognathic Diseases [C07]
- Mouth Diseases [C07.465]

Stomatognathic Diseases [C07]
- Mouth Diseases [C07.465]
  - Facial Nerve Diseases [C07.465.299]

Nervous System Diseases [C10]
- Cranial Nerve Diseases [C10.292]
  - Facial Nerve Diseases [C10.292.319]

Facial Hemiatrophy Preferred

Concept UI: M0008116
Scope Note: A syndrome characterized by slowly progressive unilateral atrophy of facial subcutaneous fat, muscle tissue, skin, cartilage, and bone. The condition typically progresses over a period of 2-10 years and then stabilizes.
Terms: Facial Hemiatrophy Preferred Term
Term UI T015736
Date01/01/1999
LexicalTag NON
ThesaurusID NLM (1966); Romberg's Disease
Term UI T015737
Date02/14/1997
LexicalTag EPO
ThesaurusID NLM (1998); Romberg Disease
Term UI T015738
Date03/30/1974
LexicalTag EPO
ThesaurusID UNK (19XX); Hemifacial Atrophy
Term UI T370407
Date11/03/1999
LexicalTag NON
ThesaurusID NLM (2000); Facial Hemiatrophy of Romberg
Term UI T370408
Date11/03/1999
LexicalTag EPO
ThesaurusID NLM (2000); Parry-Romberg Syndrome
Term UI T370409
Date11/03/1999
LexicalTag EPO
ThesaurusID; Parry-Romberg Disease
Term UI T370410
Date11/03/1999
LexicalTag EPO
ThesaurusID NLM (2000); Progressive Facial Hemiatrophy
Term UI T370411
Date11/03/1999
LexicalTag NON
ThesaurusID NLM (2000); Progressive Hemifacial Atrophy
Term UI T370412
Date11/03/1999
LexicalTag NON
ThesaurusID; Romberg Hemi-Facial Atrophy
Term UI T769770
Date04/19/2010
LexicalTag EPO
ThesaurusID; Hemifacial Atrophy, Progressive
Term UI T811526
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013)

Facial Hemiatrophy MeSH Descriptor Data 2024