Hemifacial atrophy
Symptom Information:
Symptom ID: | HPO:0011331 | ||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |