Decreased muscle mass
Symptom Information:
Symptom ID: | HPO:0003199 | ||||
Synonyms: |
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Quality: | |||||
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 morphology(HPO:0011805) Decreased muscle mass(HPO:0003199) MedDRA: |
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Database Frequency: | 27 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
ARTHROGRYPOSIS, DISTAL, WITH MENTAL RETARDATION AND CHARACTERISTICFACIES | (OMIM:208081) |
Arthrogryposis with oculomotor limitation and electroretinal anomalies | (Orphanet:1154) |
Bifunctional enzyme deficiency | (Orphanet:300) |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R | (OMIM:615490) |
EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE | (OMIM:608763) |
Faciocardiorenal syndrome | (Orphanet:1973) |
Glycogen storage disease due to glucose-6-phosphatase deficiency | (Orphanet:364) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
Intellectual deficit, X-linked, Brooks type | (Orphanet:3056) |
Intellectual deficit, X-linked, Snyder type | (Orphanet:3063) |
Isolated follicle stimulating hormone deficiency | (Orphanet:52901) |
Leprechaunism | (Orphanet:508) |
MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGEDAPPEARANCE | (OMIM:248010) |
MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:608931) |
Marden-Walker syndrome | (Orphanet:2461) |
Marfan syndrome type 1 | (Orphanet:284963) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Pantothenate kinase-associated neurodegeneration | (Orphanet:157850) |
Prader-Willi syndrome | (Orphanet:739) |
RIENHOFF SYNDROME | (OMIM:615582) |
SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE | (OMIM:613744) |
Synaptic congenital myasthenic syndromes | (Orphanet:98915) |
WARBURG MICRO SYNDROME 4 | (OMIM:615663) |
Wilson-Turner syndrome | (Orphanet:3459) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |