Internal nuclei

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Internal nuclei" [OMIM:Internal nuclei]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant limb-girdle muscular dystrophy type 1D (Orphanet:34516)
Congenital myopathy with internal nuclei and atypical cores (Orphanet:319160)
MYOPATHY, DISTAL, TATEYAMA TYPE (OMIM:614321)
MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET (OMIM:300718)
MYOPATHY, REDUCING BODY, X-LINKED, EARLY-ONSET, SEVERE (OMIM:300717)
Muscular dystrophy, Selcen type (Orphanet:199340)
Myosclerosis (Orphanet:289380)
Vici syndrome (Orphanet:1493)
ZASP-related myofibrillar myopathy (Orphanet:98912)