Hypomimic face
Symptom Information:
Symptom ID: | HPO:0000338 | ||||||||
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 the musculature(HPO:0003011) Abnormality of facial musculature(HPO:0000301) Hypomimic face(HPO:0000338) 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) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Cortical dysfunction NEC(MedDRA:10011168) Hypomimic face(HPO:0000338) |
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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) |