Congenital muscular dystrophy

Symptom Information:

Symptom ID: HPO:0003741
Synonyms:
Muscular dystrophy, congenital [HPO:0003741]
Congenital muscular dystrophy [OMIM:Congenital muscular dystrophy]
Muscular dystrophy, congenital [OMIM:Muscular dystrophy, congenital]
Quality:
Cross references:
OMIM: "Congenital muscular dystrophy" [OMIM:Congenital muscular dystrophy]
OMIM: "Muscular dystrophy, congenital" [OMIM:Muscular dystrophy, congenital]
Is a (Direct Parents):
HPO         Muscular dystrophy
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle morphology(HPO:0011805)
             Muscular dystrophy(HPO:0003560)
                Congenital muscular dystrophy(HPO:0003741)
MedDRA:
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

Arthrogryposis due to muscular dystrophy (Orphanet:1155)
Autosomal recessive limb-girdle muscular dystrophy type 2I (Orphanet:34515)
Congenital muscular dystrophy - infantile cataract - hypogonadism (Orphanet:1875)
Congenital muscular dystrophy due to LMNA mutation (Orphanet:157973)
Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect (Orphanet:280671)
Congenital muscular dystrophy type 1A (Orphanet:258)
Congenital muscular dystrophy type 1B (Orphanet:98893)
Congenital muscular dystrophy with cerebellar involvement (Orphanet:370959)
Congenital muscular dystrophy with integrin alpha-7 deficiency (Orphanet:34520)
Congenital muscular dystrophy, Ullrich type (Orphanet:75840)
Early-onset myopathy with fatal cardiomyopathy (Orphanet:289377)
MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE (OMIM:609456)
MUSCULAR DYSTROPHY, CONGENITAL, WITH RAPID PROGRESSION (OMIM:254100)
MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEMATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS (OMIM:601170)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 4 (OMIM:253800)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 1 (OMIM:613155)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 14 (OMIM:615351)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 2 (OMIM:613156)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 3 (OMIM:613151)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 6 (OMIM:608840)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION),TYPE B, 4 (OMIM:613152)
Muscle-eye-brain disease (Orphanet:588)