Decreased muscle mass

Symptom Information:

Symptom ID: HPO:0003199
Synonyms:
Underdeveloped muscles [HPO:0003199]
Decreased muscle mass [OMIM:Decreased muscle mass]
Underdeveloped muscles [OMIM:Underdeveloped muscles]
Decreased muscle mass (especially in lower limbs) [OMIM:Decreased muscle mass (especially in lower limbs)]
Quality:
Cross references:
OMIM: "Decreased muscle mass" [OMIM:Decreased muscle mass]
OMIM: "Underdeveloped muscles" [OMIM:Underdeveloped muscles]
OMIM: "Decreased muscle mass (especially in lower limbs)" [OMIM:Decreased muscle mass (especially in lower limbs)]
Is a (Direct Parents):
HPO         Abnormality of muscle morphology
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:
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)