has material basis in germline mutation in NSDHL bone benign neoplasm melanocytic nevus CHILD syndrome https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/4948 https://rarediseases.info.nih.gov/diseases/6039/child-syndrome https://www.malacards.org/card/congenital_hemidysplasia_with_ichthyosiform_erythroderma_and_limb_defects ichthyosiform erythroderma, unilateral, with ipsilateral malformations, especially absence deformity of limbs GARD:0006039 CHILD syndrome, X-linked dominant NANDO:2201358 Ichthyosis, CHILD Syndrome DOID:0111822 ICD9:759.89 MEDGEN:82697 congenital hemidysplasia with ichthyosiform nevus and limb defects MONDO:0010621 OMIM:308050 Orphanet:139 ichthyosis, child syndrome UMLS:C0265267 child nevus CHILD syndrome (Congenital Hemidysplasia with Ichthyosiform nevus and Limb Defects, CS) is an X-linked dominant genodermatosis characterized by unilateral inflammatory and scaling skin lesions with ipsilateral visceral and limb anomalies. child syndrome SCTID:17608003 CHILD syndrome NORD:1284 NANDO:1200629 NANDO:2200998 MESH:C562515 congenital hemidysplasia with ichthyosiform erythroderma and limb defects multiple congenital anomalies/dysmorphic syndrome without intellectual disability syndromic dyslipidemia X-linked ichthyosis syndrome sterol biosynthesis disorder chondrodysplasia punctata hereditary disorder of connective tissue hereditary skin disorder