Hypomimic face

Symptom Information:

Symptom ID: HPO:0000338
Synonyms:
Expressionless face [Orphanet:3180]
Masklike facies (finding) [Orphanet:3180]
Expressionless face (finding) [Orphanet:3180]
Amimia [Orphanet:3180]
Mask-like facies [Orphanet:3180]
Hypomimic face [OMIM:Hypomimic face]
Expressionless face/amimia [Orphanet:3180]
Amimia [MedDRA:10053238]
Quality:
Cross references:
HPO:0008769 "Dull facial expression" [Orphanet:3180]
HPO:0000298 "Mask-like facies" [Orphanet:3180]
HPO:0004673 "Decreased facial expression" [Orphanet:3180]
Orphanet:3180 "Expressionless face/amimia" [Orphanet:3180]
OMIM: "Hypomimic face" [OMIM:Hypomimic face]
UMLS:C1095926 "Amimia" [Orphanet:3180]
UMLS:C0813217 "Expressionless face" [Orphanet:3180]
UMLS:C0424448 "Mask-like facies" [Orphanet:3180]
Is a (Direct Parents):
MedDRA Cortical dysfunction NEC
Orphanet Abnormal facial shape
HPO         Abnormality of facial musculature
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)
                Abnormality of facial soft tissue(HPO:0011799)
                   Abnormality of facial musculature(HPO:0000301)
                      Hypomimic face(HPO:0000338)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of facial musculature(HPO:0000301)
             Hypomimic face(HPO:0000338)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Neurological disorders NEC(MedDRA:10029305)
       Cortical dysfunction NEC(MedDRA:10011168)
          Hypomimic face(HPO:0000338)
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Adult polyglucosan body disease (Orphanet:206583)
Choanal atresia - deafness - cardiac defects - dysmorphism (Orphanet:1200)
MELAS (Orphanet:550)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3 (OMIM:608443)
Menkes disease (Orphanet:565)
Neurodegeneration with brain iron accumulation due to C19orf12 mutation (Orphanet:289560)
Rapid-onset dystonia-parkinsonism (Orphanet:71517)
Steinert myotonic dystrophy (Orphanet:273)