Hemifacial atrophy

Symptom Information:

Symptom ID: HPO:0011331
Synonyms:
Facial hemiatrophy [Orphanet:3300]
Facial Hemiatrophy [Orphanet:3300]
Facial structural asymmetry/facial hemiatrophy/facial hemihypertrophy [Orphanet:3300]
Progressive facial hemiatrophy [MedDRA:10073006]
Facial hemiatrophy [MedDRA:10073006]
Parry-Romberg's disease [MedDRA:10073006]
Quality:
Cross references:
Orphanet:3300 "Facial structural asymmetry/facial hemiatrophy/facial hemihypertrophy" [Orphanet:3300]
UMLS:C0015458 "Facial Hemiatrophy" [Orphanet:3300]
Is a (Direct Parents):
Orphanet Abnormal facial shape
Orphanet Hemifacial hypertrophy
HPO         Facial asymmetry
MedDRA Skin autoimmune disorders NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormal facial shape(HPO:0001999)
                   Facial asymmetry(HPO:0000324)
                      Hemifacial atrophy(HPO:0011331)
MedDRA:
Immune system disorders(MedDRA:10021428)
    Autoimmunity(HPO:0002960)
       Skin autoimmune disorders NEC(MedDRA:10052738)
          Hemifacial atrophy(HPO:0011331)
Database Frequency: 79 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
2q31.1 microdeletion syndrome (Orphanet:251014)
2q32q33 microdeletion syndrome (Orphanet:251019)
3q29 microdeletion syndrome (Orphanet:65286)
48,XXXY syndrome (Orphanet:96263)
48,XXYY syndrome (Orphanet:10)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Aortic arch anomaly - peculiar facies - intellectual deficit (Orphanet:1110)
Apert syndrome (Orphanet:87)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Axial mesodermal dysplasia spectrum (Orphanet:1834)
Bencze syndrome (Orphanet:1241)
Blepharophimosis - radioulnar synostosis (Orphanet:1256)
Branchio-otic syndrome (Orphanet:52429)
CHARGE syndrome (Orphanet:138)
CLAPO syndrome (Orphanet:168984)
Caffey disease (Orphanet:1310)
Camptodactyly - joint contractures - facial skeletal defects (Orphanet:1323)
Cleft lip/palate - deafness - sacral lipoma (Orphanet:2003)
Cleft palate - short stature - vertebral anomalies (Orphanet:2015)
Congenital unilateral hypoplasia of depressor anguli oris (Orphanet:1166)
Craniofacial dyssynostosis (Orphanet:1516)
Craniofrontonasal dysplasia (Orphanet:1520)
Curry-Jones syndrome (Orphanet:1553)
Deafness - genital anomalies - metacarpal and metatarsal synostosis (Orphanet:3224)
Deafness-craniofacial syndrome (Orphanet:3241)
Delayed speech - facial asymmetry - strabismus - ear lobe creases (Orphanet:3038)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal trisomy 15q (Orphanet:1707)
Dysmorphism - short stature - deafness - disorder of sex development (Orphanet:2282)
Epiphyseal dysplasia - hearing loss - dysmorphism (Orphanet:1825)
Erythrokeratodermia - ataxia (Orphanet:1955)
Familial lambdoid synostosis (Orphanet:3267)
Fanconi anemia (Orphanet:84)
Fine-Lubinsky syndrome (Orphanet:1272)
Focal dermal hypoplasia (Orphanet:2092)
Fronto-facio-nasal dysostosis (Orphanet:1791)
Goldenhar syndrome (Orphanet:374)
Gordon syndrome (Orphanet:376)
Grant syndrome (Orphanet:2097)
Hemihypertrophy (Orphanet:2128)
Holoprosencephaly - craniosynostosis (Orphanet:2163)
Hypertrichosis cubiti - short stature (Orphanet:2220)
Hypoglossia - hypodactyly (Orphanet:989)
Intellectual deficit - athetosis - microphthalmia (Orphanet:1236)
Intellectual deficit - myopathy - short stature - endocrine defect (Orphanet:3068)
Intellectual deficit, X-linked, Miles-Carpenter type (Orphanet:85283)
Isolated Klippel-Feil syndrome (Orphanet:2345)
Isolated plagiocephaly (Orphanet:35098)
Jacobsen syndrome (Orphanet:2308)
KBG syndrome (Orphanet:2332)
Kleefstra syndrome (Orphanet:261494)
Linear nevus sebaceus syndrome (Orphanet:2612)
Malignant hyperthermia - arthrogryposis - torticollis (Orphanet:2215)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Microcephaly - deafness - intellectual deficit (Orphanet:2533)
Multiple synostoses syndrome (Orphanet:3237)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Neurogenic arthrogryposis multiplex congenita (Orphanet:1143)
Oculoauriculovertebral spectrum with radial defects (Orphanet:2549)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 5 (Orphanet:2919)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Otofaciocervical syndrome (Orphanet:2792)
Pfeiffer syndrome (Orphanet:710)
Phakomatosis pigmentovascularis (Orphanet:2875)
Pilotto syndrome (Orphanet:2894)
Progressive hemifacial atrophy (Orphanet:1214)
Saethre-Chotzen syndrome (Orphanet:794)
Tel Hashomer camptodactyly syndrome (Orphanet:3292)
Temtamy syndrome (Orphanet:1777)
Tetrasomy 18p (Orphanet:3307)
Torticollis - keloids - cryptorchidism - renal dysplasia (Orphanet:3341)
Townes-Brocks syndrome (Orphanet:857)
Triopia (Orphanet:3374)
Velo-facial-skeletal syndrome (Orphanet:3424)
Wildervanck syndrome (Orphanet:3456)
Wrinkly skin syndrome (Orphanet:2834)
X-linked mandibulofacial dysostosis (Orphanet:1131)