Polygenic inheritance
Symptom Information:
Symptom ID: | HPO:0010982 | ||||||
Synonyms: |
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Quality: | |||||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Mode of inheritance(HPO:0000005) Multifactorial inheritance(HPO:0001426) Polygenic inheritance(HPO:0010982) MedDRA: |
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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) |