syndromic disease microcephaly-complex motor and sensory axonal neuropathy syndrome https://github.com/monarch-initiative/mondo/issues/6752 https://github.com/monarch-initiative/mondo/issues/6877 https://www.malacards.org/card/microcephaly_complex_motor_and_sensory_axonal_neuropathy_syndrome UMLS:C4706585 Microcephaly-complex motor and sensory axonal neuropathy syndrome is an extremely rare subtype of hereditary motor and sensory neuropathy characterized by severe, rapidly-progressing, distal, symmetric polyneuropathy and microcephaly (which can be evident in utero) with intact cognition. Clinically it presents with delayed motor development, hypotonia, absent or reduced deep tendon reflexes, progressive muscle wasting and weakness and scoliosis. MONDO:0018507 GARD:0021762 Orphanet:423894 MEDGEN:1637079 hereditary neurological disease