| 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 |