Disease #04287 (myopathy, myofibrillar, fatal infantile hypertrophy, alpha-B crystallin-related, OMIM:613869)

Official abbreviation -
Name myopathy, myofibrillar, fatal infantile hypertrophy, alpha-B crystallin-related
OMIM ID 613869
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CRYAB
Associated tissues -
Disease features -
Remarks -