scalp–ear–nipple syndrome
human disease
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Summary
scalp–ear–nipple syndrome is a malformation syndrome[1]. It draws 484 Wikipedia views per month (malformation_syndrome category, ranking #9 of 8).[2]
Key Facts
- scalp–ear–nipple syndrome's instance of is recorded as malformation syndrome[3].
- scalp–ear–nipple syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- scalp–ear–nipple syndrome's instance of is recorded as rare disease[5].
- scalp–ear–nipple syndrome's instance of is recorded as class of disease[6].
- scalp–ear–nipple syndrome is a type of ectodermal dysplasia[7].
- scalp–ear–nipple syndrome is a type of multiple congenital anomalies/dysmorphic syndrome without intellectual disability[8].
- scalp–ear–nipple syndrome is a type of deficient breast volume or number[9].
- scalp–ear–nipple syndrome is a type of rare genetic gynecological and obstetrical diseases[10].
- scalp–ear–nipple syndrome is a type of mixed dermis disorder[11].
- scalp–ear–nipple syndrome is a type of autosomal dominant disease[12].
- scalp–ear–nipple syndrome's genetic association is recorded as KCTD1[13].
- scalp–ear–nipple syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2036[14].
- scalp–ear–nipple syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111550[15].
- scalp–ear–nipple syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111550[16].
Why It Matters
scalp–ear–nipple syndrome draws 484 Wikipedia views per month (malformation_syndrome category, ranking #9 of 8).[2] It is known by 11 alternative names across languages and contexts.[17]