Polygenic inheritance

Symptom Information:

Symptom ID: HPO:0010982
Synonyms:
Polygenic/multifactorial inheritance [Orphanet:52300]
Quality:
Cross references:
Orphanet:52300 "Polygenic/multifactorial inheritance" [Orphanet:52300]
Is a (Direct Parents):
Orphanet Multifactorial inheritance
Orphanet Cytogenetic abnormality
HPO         Multifactorial inheritance
Is a (Whole tree): HPO:
All(HPO:0000001)
    Mode of inheritance(HPO:0000005)
       Multifactorial inheritance(HPO:0001426)
          Polygenic inheritance(HPO:0010982)
MedDRA:
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

ARM FOLDING PREFERENCE (OMIM:107850)
CAROTID INTIMAL MEDIAL THICKNESS 1 (OMIM:609338)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO (OMIM:612551)
GALLBLADDER DISEASE 4 (OMIM:611465)
LEUKEMIA, ACUTE LYMPHOBLASTIC (OMIM:613065)
MACULAR DEGENERATION, AGE-RELATED, 11 (OMIM:611953)
MACULAR DEGENERATION, AGE-RELATED, 4 (OMIM:610698)
NASOPHARYNGEAL CARCINOMA (OMIM:607107)
OROFACIAL CLEFT 6, SUSCEPTIBILITY TO (OMIM:608864)
PREECLAMPSIA/ECLAMPSIA 4 (OMIM:609404)
PRETERM PREMATURE RUPTURE OF THE MEMBRANES (OMIM:610504)
SCHIZOPHRENIA 15 (OMIM:613950)
SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 6 (OMIM:609939)
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (OMIM:606579)