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