Hipofosfatemia Familiar

Preferred Label : Hipofosfatemia Familiar;

Wikipedia automatic translation : Hipofosfatemia;

Wikipedia link : https://es.wikipedia.org/wiki/Hipofosfatemia;

Details

Origin ID

D007015;

UMLS CUI

C0020631;

False automatic mappings
- Raquitismo hipofosfatémico autosómico dominante [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Displasia ósea primaria con mineralización ósea defectuosa [ORDO Disease]
- Raquitismo hipofosfatémico hereditario con hipercalciuria [ORDO Disease]
MeSH Descriptor(s) used for indexing
- Hipofosfatemia [MeSH Descriptor]
See also (suggested by CISMeF)
- Hipofosfatemia [MeSH Descriptor]
- Raquitismo [MeSH Descriptor]
UMLS correspondences (same concept)
- Raquitismo hipocalcémico [ORDO Disease]

Keyword's position in hierarchy(ies) :

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