Facial hypotonia
Symptom Information:
Symptom ID: | HPO:0000297 | ||||
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 muscle physiology(HPO:0011804) Abnormal muscle tone(HPO:0003808) Muscular hypotonia(HPO:0001252) Facial hypotonia(HPO:0000297) Abnormality of facial musculature(HPO:0000301) Facial hypotonia(HPO:0000297) 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) Facial hypotonia(HPO:0000297) MedDRA: |
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Database Frequency: | 8 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Cohen syndrome | (Orphanet:193) |
Intellectual deficit, X-linked - psychosis - macroorchidism | (Orphanet:3077) |
LUBS X-LINKED MENTAL RETARDATION SYNDROME | (OMIM:300260) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Pontocerebellar hypoplasia, type 9 | (OMIM:615809) |
SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE | (OMIM:613744) |
Syndromic X-linked intellectual deficit due to JARID1C mutation | (Orphanet:85279) |
X-linked spastic paraplegia type 16 | (Orphanet:100997) |