Preferred Name |
Facioscapulohumeral muscular dystrophy 1a |
Synonyms |
Muscular dystrophy, facioscapulohumeral, type 1a |
ID |
http://purl.bioontology.org/ontology/MESH/C536391 |
altLabel |
Muscular dystrophy, facioscapulohumeral, type 1a FSHD1A Facioscapulohumeral dystrophy with sensorineural hearing loss and tortuosity of retinal arterioles Facioscapulohumeral muscular dystrophy, infantile FSHMD1A Landouzy-dejerine muscular dystrophy |
cui |
C1834673 |
HM |
D020391 |
Inverse of RB |
0 |
Mapped to | |
MDA |
20100825 |
MeSH Frequency |
14 |
MMR |
20121105 |
notation |
C536391 |
prefLabel |
Facioscapulohumeral muscular dystrophy 1a |
SC |
3 |
Scope Statement |
PROM |
TERMUI |
T760273 T739180 T739184 T760272 T739181 T739185 T739183 |
TH |
ORD (2010) OMIM (2013) |
tui |
T047 |
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.bioontology.org/ontology/OMIM/158900 | Online Mendelian Inheritance in Man | CUI |