Hyporeflexia or areflexia

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Hyporeflexia or areflexia" [OMIM:Hyporeflexia or areflexia]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) (OMIM:214100)
Severe X-linked mitochondrial encephalomyopathy (Orphanet:238329)