Facial hypotonia

Symptom Information:

Symptom ID: HPO:0000297
Synonyms:
Facial hypotonia [OMIM:Facial hypotonia]
Quality:
Cross references:
OMIM: "Facial hypotonia" [OMIM:Facial hypotonia]
Is a (Direct Parents):
HPO         Abnormality of facial musculature
HPO         Muscular hypotonia
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)
                      Facial hypotonia(HPO:0000297)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of facial musculature(HPO:0000301)
             Facial hypotonia(HPO:0000297)
          Abnormality of muscle physiology(HPO:0011804)
             Abnormal muscle tone(HPO:0003808)
                Muscular hypotonia(HPO:0001252)
                   Facial hypotonia(HPO:0000297)
MedDRA:
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)