Multifactorial inheritance

Symptom Information:

Symptom ID: HPO:0001426
Synonyms:
Polygenic/multifactorial inheritance [Orphanet:52300]
Quality:
Cross references:
Orphanet:52300 "Polygenic/multifactorial inheritance" [Orphanet:52300]
Is a (Direct Parents):
HPO         Mode of inheritance
Orphanet Cytogenetic abnormality
Is a (Whole tree): HPO:
All(HPO:0000001)
    Mode of inheritance(HPO:0000005)
       Multifactorial inheritance(HPO:0001426)
MedDRA:
Database Frequency: 37 / 7739
Resource:

All diseases associated with this symptom:

15q11q13 microduplication syndrome (Orphanet:238446)
ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1 (OMIM:608638)
ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2 (OMIM:608631)
ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (OMIM:300494)
ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2 (OMIM:300497)
AUTISM (OMIM:209850)
AUTISM, SUSCEPTIBILITY TO, 3 (OMIM:608049)
AUTISM, SUSCEPTIBILITY TO, 8 (OMIM:607373)
AUTISM, SUSCEPTIBILITY TO, X-LINKED 1 (OMIM:300425)
AUTISM, SUSCEPTIBILITY TO, X-LINKED 2 (OMIM:300495)
AUTISM, SUSCEPTIBILITY TO, X-LINKED 3 (OMIM:300496)
Alopecia totalis (Orphanet:700)
Arnold-Chiari malformation type II (Orphanet:1136)
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 (OMIM:612555)
BULIMIA NERVOSA, SUSCEPTIBILITY TO, 1 (OMIM:607499)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
CYCLIC VOMITING SYNDROME (OMIM:500007)
Congenital diaphragmatic hernia (Orphanet:2140)
Congenital velopharyngeal incompetence (Orphanet:2291)
DEVELOPMENTAL DYSPLASIA OF THE HIP 1 (OMIM:142700)
DYSLEXIA, SUSCEPTIBILITY TO, 8 (OMIM:608995)
ENDOMETRIOSIS, SUSCEPTIBILITY TO, 1 (OMIM:131200)
HYPERLEXIA (OMIM:238350)
HYPERTENSION, ESSENTIAL (OMIM:145500)
Hereditary breast and ovarian cancer syndrome (Orphanet:145)
INFLAMMATORY BOWEL DISEASE 1 (OMIM:266600)
INFLAMMATORY BOWEL DISEASE 11 (OMIM:191390)
LIP PRINTS (OMIM:247150)
MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO (OMIM:126200)
OSTEOARTHRITIS SUSCEPTIBILITY 1 (OMIM:165720)
PSORIASIS 1, SUSCEPTIBILITY TO (OMIM:177900)
PYGMY (OMIM:265850)
PYLORIC STENOSIS, INFANTILE HYPERTROPHIC, 1 (OMIM:179010)
SPECIFIC LANGUAGE IMPAIRMENT 1 (OMIM:606711)
SPECIFIC LANGUAGE IMPAIRMENT 2 (OMIM:606712)
SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1 (OMIM:106300)
TRICHOTILLOMANIA (OMIM:613229)